NAD+ legality varies by country. Of 158 countries tracked: 122 legal, 20 grey area, 3 prescription, 13 banned.

Do I need a prescription for NAD+?

Yes, 1 of 158 countries require a prescription for NAD+. Including: Cuba, Aruba, United Arab Emirates.

Is NAD+ Legal? Global Status Guide

Q: Where is NAD+ banned?

NAD+ is banned in 13 countries: Vietnam, Zambia, Botswana, Senegal, Cameroon, Paraguay, Costa Rica, Bolivia, Uruguay, Venezuela, Guyana, Belize, Trinidad and Tobago.

Q: Where is NAD+ legal?

NAD+ is fully legal in 122 countries: United Kingdom, France, Grenada, Italy, Philippines, Indonesia, St Lucia, Anguilla, and 114 more.

Category: Longevity · Tracked in 158 countries

122

Legal

Grey Area

Prescription

Banned

Can You Buy NAD+?

Whether you can buy NAD+ depends on your country. It is legal to purchase in 122 countries, including United Kingdom, France, Grenada, Italy, Philippines, Indonesia, St Lucia, Anguilla, and 114 more. A prescription is required in 3 countries, including Cuba, Aruba, United Arab Emirates. It falls into a legal grey area in 20 countries (Zimbabwe, Sint Eustatius, Andorra, Bahamas, Barbados, St Kitts and Nevis, Montserrat, Turks and Caicos, and 12 more), where it may be available for research but not for human use. It is banned in 13 countries: Vietnam, Zambia, Botswana, Senegal, Cameroon, Paraguay, Costa Rica, Bolivia, and 5 more.

Traveling with NAD+

Traveling internationally with NAD+ requires understanding local laws at your destination. Do not carry NAD+ into countries where it is banned (Vietnam, Zambia, Botswana, Senegal, Cameroon, Paraguay, Costa Rica, Bolivia, and 5 more) — you could face serious legal consequences. In countries requiring a prescription (Cuba, Aruba, United Arab Emirates), carry a valid prescription or doctor's letter. Always declare pharmaceutical products at customs and check the latest regulations before traveling.

Need to calculate your NAD+ dosage? Use the NAD+ reconstitution calculator on peptide.locker

NAD+ Legal Status by Country (158)

Country	Status	Rx Required	Schedule	Detail	Source
Algeria	Legal	No	Supplement	NAD+ supplements not classified as medicines under Law 18-11. Available through import. OTC classification possible for supplements with proven safety.	Secondary
Angola	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import. Minimal supplement regulation.	Secondary
Anguilla	Legal	No	Supplement	Available as supplement. No restrictions.	Unsourced
Argentina	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
Australia	Legal	No	Not Scheduled	NAD+ precursors (NMN, NR) available as supplements. IV NAD+ infusions offered at wellness clinics. Not specifically restricted by TGA for supplement use.	Secondary
Austria	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
Bahrain	Legal	No	Supplement	Available as supplement.	Official
Belgium	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
Bosnia and Herzegovina	Legal	No	Supplement	Non-EU. NAD+ precursors sold as supplements. Not subject to EU Novel Food regulation.	Official
Brazil	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
British Virgin Islands	Legal	No	Supplement	Available as supplement. No restrictions.	Official
Bulgaria	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food. IV infusions available at wellness clinics.	Official
Cambodia	Legal	No	Supplement	Available as supplement. No restrictions.	Official
Canada	Legal	No	Not Scheduled	NAD+ precursors (NMN/NR) sold as Natural Health Products with NPN numbers. IV infusions available at clinics. Not specifically restricted.	Official
Cape Verde	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import. ARFA oversees food products including supplements.	Secondary
Cayman Islands	Legal	No	Supplement	Available as supplement. No specific restrictions.	Secondary
Chile	Legal	No	Supplement	Available as supplement. No specific restrictions. Framework: Decreto Supremo 3/2010 art. 20 requires prior sanitary registration for any pharmaceutical product distributed or used in Chile on any basis. The personal-import exception in art. 21(b) is conditioned by art. 21A and art. 22 on the product holding a marketing authorisation in its country of origin and on a prescription, and is capped at six months of treatment.	Official
Colombia	Legal	No	Supplement	No INVIMA sanitary registration as an injectable. NAD+ 10 mg/mL solution was named in INVIMA's 25 Jun 2026 alert as an unregistered, fraudulent product being sold through social media and messaging apps.	Secondary
Croatia	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
Cyprus	Legal	No	Not Scheduled	NAD+ precursors (NR) available as food supplements under EU framework. NMN classified as Novel Food requiring EFSA authorization (pending). IV infusions available at private clinics.	Official
Czech Republic	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025). As an EU member state, Article 6(1) of Directive 2001/83/EC applies: no medicinal product may be placed on the market of a Member State unless a marketing authorisation has been issued by the competent authorities of that Member State or under the centralised procedure. No EU or national marketing authorisation for this substance was identified, so it is an unauthorised medicinal product. National regulator: SUKL (Czechia) / EOF (Greece). Country-specific offence provisions and penalties have NOT been verified for this jurisdiction.	Official
Democratic Republic of Congo	Legal	No	Supplement	NAD+ supplements not classified as medicines. Minimal regulation of supplement market.	Official
Denmark	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Official
Dominica	Legal	No	Supplement	Available as supplement. No restrictions.	Unsourced
Dominican Republic	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
Ecuador	Legal	No	Supplement	Available as supplement. No specific restrictions.	Secondary
Egypt	Legal	No	Supplement	Available as supplement.	Official
El Salvador	Legal	No	Supplement	Available as supplement. No specific restrictions.	Secondary
Estonia	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
Ethiopia	Legal	No	Supplement	NAD+ supplements (NMN/NR) not specifically regulated as medicines. Available through import. Supplement regulation less strict than pharmaceuticals.	Official
Fiji	Legal	No	Supplement	Available as supplement. No specific restrictions on NAD+ or precursors.	Official
Finland	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Official
France	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Unofficial
French Guiana	Legal	No	Supplement	Supplement under French/EU rules.	Official
Georgia	Legal	No	Supplement	Non-EU. NAD+ precursors sold as supplements. No EU Novel Food framework applies. Widely available.	Official
Germany	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025). Unauthorised medicinal product under the Arzneimittelgesetz (AMG); placing on the market or unlicensed trade is punishable under AMG s.95. Criminal doping liability under the AntiDopG arises only for substances named in its annex, which is a closed list.	Official
Ghana	Legal	No	Supplement	NAD+ supplements available through import. FDA Ghana regulates food supplements under separate framework.	Official
Greece	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025). As an EU member state, Article 6(1) of Directive 2001/83/EC applies: no medicinal product may be placed on the market of a Member State unless a marketing authorisation has been issued by the competent authorities of that Member State or under the centralised procedure. No EU or national marketing authorisation for this substance was identified, so it is an unauthorised medicinal product. National regulator: SUKL (Czechia) / EOF (Greece). Country-specific offence provisions and penalties have NOT been verified for this jurisdiction.	Official
Grenada	Legal	No	Supplement	Available as supplement. No restrictions.	Unsourced
Guatemala	Legal	No	Supplement	Available as supplement. No specific restrictions.	Secondary
Honduras	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
Hong Kong	Legal	No	Supplement	Available as supplement.	Official
Hungary	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
Iceland	Legal	No	Supplement	NAD+ supplements follow EU dietary supplement framework. Not classified as medicine. Available commercially.	Official
India	Legal	No	Supplement	Supplements widely available. IV clinics in major cities.	Official
Indonesia	Legal	No	Supplement	IV NAD+ available at Bali wellness clinics. Growing market.	Official
Ireland	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
Israel	Legal	No	Supplement	Supplements available. IV clinics operate.	Official
Italy	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
Ivory Coast	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import.	Official
Jamaica	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
Japan	Legal	No	Supplement	NMN supplements popular in Japan. Oral supplements available. IV requires medical supervision.	Official
Jordan	Legal	No	Supplement	Available as supplement.	Official
Kenya	Legal	No	Supplement	NAD+ supplements available in Kenya through retailers (Western Cosmetics, Healthy U Nairobi). Not classified as pharmaceutical. Sold freely as dietary supplement.	Unofficial
Kuwait	Legal	No	Supplement	Available as supplement.	Official
Laos	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
Latvia	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
Libya	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import. Minimal supplement regulation.	Secondary
Liechtenstein	Legal	No	Not Scheduled	NAD+ precursors available as food supplements under EU/EEA framework. Same rules as EU member states.	Unofficial
Lithuania	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
Luxembourg	Legal	No	Not Scheduled	NAD+ precursors available as food supplements under EU framework. NMN classified as Novel Food (EFSA authorization pending). Supplement market well-regulated in Luxembourg.	Secondary
Madagascar	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import.	Official
Malawi	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import.	Official
Malaysia	Legal	No	Supplement	Available as supplement.	Official
Maldives	Legal	No	Supplement	Available as supplement. OTC items permitted in small amounts.	Official
Malta	Legal	No	Supplement	NAD+ supplements follow EU dietary supplement framework. Available commercially. Not classified as medicine.	Official
Mauritius	Legal	No	Supplement	NAD+ supplements available through import. Supplements less strictly regulated than pharmaceuticals.	Official
Mexico	Legal	No	Supplement	Available as supplement and IV drip at wellness clinics. No COFEPRIS restriction. Framework: Ley General de Salud art. 376 requires sanitary registration for medicines; unregistered products may be imported only under a COFEPRIS permit for one of the four purposes in Reglamento de Insumos para la Salud art. 132, with a personal-use permit tied to a prescription quantity. Manufacturing without the required registrations carries 3 to 15 years under LGS art. 464 Ter.	Official
Monaco	Legal	No	Not Scheduled	NAD+ precursors available as food supplements under EU/French framework. Same availability as France.	Official
Montenegro	Legal	No	Supplement	Non-EU. NAD+ precursors sold as supplements. Not subject to EU Novel Food regulation. Widely available.	Official
Morocco	Legal	No	Supplement	NAD+ supplements (oral) available through import and some local retailers. Supplement import requires compliance with labeling and composition requirements per Moroccan law. Not classified as pharmaceutical.	Secondary
Mozambique	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import.	Secondary
Myanmar	Legal	No	Supplement	Available as supplement. No restrictions.	Official
Namibia	Legal	No	Supplement	NAD+ supplements available through import, likely from SA retailers. Not classified as pharmaceutical.	Official
Nepal	Legal	No	Supplement	Available as supplement. Category GA (OTC).	Official
Netherlands	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
New Zealand	Legal	No	Supplement	NMN supplements available. IV at clinics.	Official
Nicaragua	Legal	No	Supplement	Available as supplement. No specific restrictions.	Unofficial
Nigeria	Legal	No	Supplement	NAD+ supplements available through import. NAFDAC regulates food supplements but with less scrutiny than pharmaceuticals.	Official
North Macedonia	Legal	No	Supplement	Non-EU. NAD+ precursors sold as supplements. Not subject to EU Novel Food regulation.	Secondary
Norway	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Official
Oman	Legal	No	Supplement	Available as supplement.	Official
Panama	Legal	No	Supplement	IV infusions at wellness clinics. Supplements freely available.	Secondary
Papua New Guinea	Legal	No	Not Scheduled	NAD+ supplements not specifically regulated. No local market. Import likely unimpeded due to minimal customs enforcement for supplements.	Official
Peru	Legal	No	Supplement	Available as supplement. No specific restrictions.	Secondary
Philippines	Legal	No	Supplement	Available as supplement.	Official
Poland	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025). Poland has no simple-possession offence, but the Ustawa o zwalczaniu dopingu w sporcie (Dz.U. 2017 poz. 1051) art. 49(1) criminalises making WADA group S1/S2/S4 substances available to third parties whether or not for payment, or holding them for that purpose, and art. 49(3) makes importing them contrary to Prawo farmaceutyczne art. 68 a standalone offence. Penalties: fine, restriction of liberty, or up to 3 years. Regulator: POLADA.	Official
Portugal	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
Qatar	Legal	No	Supplement	Available as supplement.	Official
Romania	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) widely sold as supplements. NR authorized as novel food in EU (Niagen). NMN pending EFSA assessment. IV infusions at wellness clinics.	Official
Russia	Legal	No	Supplement	Supplements available.	Official
Rwanda	Legal	No	Supplement	NAD+ supplements available through import. Rwanda FDA regulates processed foods and supplements.	Official
Saint Barthelemy	Legal	No	Supplement	Available as supplement under French/EU rules.	Official
Saint Martin (French)	Legal	No	Supplement	Available as supplement under French/EU rules.	Official
Samoa	Legal	No	Not Scheduled	Not specifically regulated. Supplements loosely controlled.	Official
Serbia	Legal	No	Supplement	Non-EU. NAD+ precursors (NMN/NR) sold as supplements. Not subject to EU Novel Food regulation. Widely available.	Official
Seychelles	Legal	No	Supplement	Available as supplement. No specific restrictions.	Official
Singapore	Legal	No	Supplement	NMN supplements available. IV requires medical facility license.	Official
Sint Maarten	Legal	No	Supplement	Available as supplement. No restrictions.	Unsourced
Slovakia	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
Slovenia	Legal	No	Supplement / Novel Food	NAD+ precursors (NMN/NR) sold as supplements. NR authorized as EU novel food.	Official
South Africa	Legal	No	Supplement	NAD+ supplements widely sold in SA (Charava, Largavita, Annique, Takealot). IV NAD+ infusions available at wellness clinics (NovaNAD+). Not scheduled. Sold as dietary supplement without restriction. Multiple SA retailers.	Unofficial
South Korea	Legal	No	Supplement	NMN/NR supplements available. IV clinics operate.	Official
Spain	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Secondary
Sri Lanka	Legal	No	Supplement	Available as supplement. Classified as borderline product.	Official
St Lucia	Legal	No	Supplement	Available as supplement. No restrictions.	Unsourced
St Vincent and the Grenadines	Legal	No	Supplement	Available as supplement. No restrictions.	Unsourced
Suriname	Legal	No	Supplement	Available as supplement. No specific restrictions.	Unsourced
Sweden	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Official
Switzerland	Legal	No	Supplement / Novel Food	Supplements (NMN/NR) widely sold. IV infusions at clinics. NMN awaiting EFSA novel food assessment (Uthever 2025).	Official
Taiwan	Legal	No	Supplement	Available as supplement.	Official
Tanzania	Legal	No	Supplement	NAD+ supplements available through import. Supplement regulation less strict than pharmaceuticals.	Official
Thailand	Legal	No	Supplement	IV NAD+ widely available at Bangkok wellness clinics. Major offering.	Official
Tonga	Legal	No	Not Scheduled	Not specifically regulated. Supplements not formally controlled.	Official
Tunisia	Legal	No	Supplement	NAD+ supplements available through import. Food supplements regulated by DPM but less strictly than medicines.	Official
Turkey	Legal	No	Supplement	Supplements available. IV clinics in Istanbul.	Official
Uganda	Legal	No	Supplement	NAD+ supplements not classified as medicines. Available through import. Supplement market loosely regulated.	Official
Ukraine	Legal	No	Supplement	Non-EU. NAD+ precursors sold as supplements. Not subject to EU Novel Food regulation. Widely available.	Official
United Kingdom	Legal	No	Not Scheduled	NAD+ supplements (NMN/NR) sold freely. IV infusions available at wellness clinics. No specific restrictions.	Unofficial
United States	Legal	No	Not Scheduled	NAD+ (nicotinamide adenine dinucleotide) has unique status. Oral supplements (NMN/NR precursors) sold freely as dietary supplements. IV NAD+ infusions offered at wellness clinics under medical supervision. Not specifically targeted by FDA for enforcement.	Secondary
US Virgin Islands	Legal	No	Not Scheduled	Same as US. Supplements and IV infusions available.	Official
Vanuatu	Legal	No	Not Scheduled	Not specifically regulated. No supplement framework.	Official
Andorra	Grey Area	No	Reconeixement Paisos Referents	Andorra is not in the EU, so EMA authorisation does not apply of its own force - but the position tracks its neighbours by statute, not merely in practice. Llei general de sanitat (20 March 1989) art. 40(1) empowers the Government to recognise directly the marketing authorisations issued by the competent authorities of the reference countries. The Reglament de Medicaments of 4 October 1977 goes further: art. 1 provides that in the absence of Andorran tables, FRENCH regulation applies, and that anything on the narcotics list of a neighbouring country is automatically in Table B; art. 10 provides that human medicines follow the MORE LIBERAL of the two neighbouring regimes for toxic and dangerous substances, and the MORE RESTRICTIVE for narcotics. In practice a peptide unauthorised in both France and Spain is unauthorised in Andorra. Custody and dispensing are reserved to authorised pharmacies (art. 46), and importers require prior authorisation (art. 43). Penalties under the health law are administrative: fines to EUR 100,000 for very serious infringements, with criminal referral preserved separately.	Official
Antigua and Barbuda	Grey Area	No	Reform Pending	Currently governed by the Pharmacy Act 1995 (as amended 2019) and the Antibiotics and Therapeutic Substances Act, Cap. 17, neither of which operates a general product-approval regime reaching peptides. A draft Pharmacy Bill 2026, published November 2025, would change this substantially: it defines unlicensed or unregistered medical products, requires imported products to be registered and approved in the country of origin and by a WHO Listed Authority or recommended by the Caribbean Regulatory System, and introduces marketing authorisation based on quality, safety and efficacy. Clause 33 targets courier and mail-order supply directly, requiring an import licence from the Council plus the original prescription from a locally registered practitioner and proof the drug is unavailable locally, with a stated maximum of three months for personal use. Clause 36 requires any injectable supplement to be prescribed. Proposed penalties are severe: EC$40,000 and 12 months generally, and a minimum EC$500,000 fine and up to 5 years for knowingly supplying substandard or falsified drugs. THIS IS A DRAFT BILL, NOT LAW - re-check enactment before relying on it.	Official
Bahamas	Grey Area	No	No Product Registration Regime	The Bahamas has NO drug marketing-authorisation system. The Pharmacy Act, Ch. 227 (Act No. 8 of 2009) registers people and premises and licenses manufacturers and wholesalers, but does not require a product to be approved before sale - claims that the Bahamas operates drug registration are incorrect. What binds instead: s.27 requires every drug manufactured, offered for sale, imported or exported to meet a pharmacopoeial standard (BP, USP, Ph. Eur., Int. Ph. or another approved by the Minister), with a fine up to BSD 20,000 - a research-grade peptide with no pharmacopoeial monograph fails that test. Section 28 refers import and export control to the Customs Management Act rather than medicines law. Section 33 requires factory and warehouse registration for manufacture or import for storage and wholesale distribution, fine up to BSD 15,000. Note also s.30(5): a prescription expressly does NOT include one transmitted electronically via the internet, which bears directly on online-prescriber models. No traveller allowance was located in the Pharmacy Act.	Official
Bangladesh	Grey Area	No	Not Scheduled	NAD+ supplements not specifically regulated. May be available through import channels. Supplement regulation less strict than pharmaceuticals.	Official
Barbados	Grey Area	No	Not Within Scheduled Substances	No product marketing-authorisation regime was located. The Barbados National Drug Formulary is a public-benefit reimbursement list, not a market authorisation - the two should not be conflated. The operative import control is the Therapeutic Substances Act, Cap. 330 (1949-40, in force 1 December 1950), s.6 of which makes it unlawful to import a drug or therapeutic substance to which the Act applies without a licence from the Licensing Authority (the Chief Medical Officer), manufacture by an approved pharmaceutical firm, and compliance with prescribed standards. BUT the Act's Schedule covers only sulphonamides, penicillin, streptomycin, oleandomycin and other antibiotic substances - a therapeutic peptide is NOT within it, so Cap. 330's import licence does not bite. The remaining constraints are the Pharmacy Act Cap. 372 (poisons and dispensing) and customs. The Cap. 330 penalty is BBD 480 or three months and has not been uprated since 1950.	Official
Bonaire	Grey Area	No	Wet Geneesmiddelenvoorziening Bes	Bonaire, Sint Eustatius and Saba are Dutch public bodies, but the Dutch Geneesmiddelenwet does NOT extend to them - the applicable statute is the separate Wet op de geneesmiddelenvoorziening BES, cited by article in Staatscourant 2025 nr. 28064. Enforcement sits with the Dutch health inspectorate (IGJ) and the Minister of VWS. An adviescommissie geneesmiddelenvoorziening BES was established on 4 August 2025, but its remit is pharmacy establishment licensing, not product approval. No BES medicines-registration provision was located, so registration status, import rules, traveller allowance and penalties remain unverified for these islands.	Official
Brunei	Grey Area	No	Not Scheduled	NAD+ supplements may fall under health supplement exemption from BDMCA pre-market authorization. Traditional medicines and health supplements currently not requiring licensing.	Official
China	Grey Area	No	Supplement (Grey Area)	Supplement market exists but regulation inconsistent.	Official
Curacao	Grey Area	No	Landsverordening Geneesmiddelenvoorziening	Curacao is an autonomous country with its own Landsverordening op de geneesmiddelenvoorziening, descended from Netherlands Antilles law - Dutch and EU medicines law do not apply. The ordinance is confirmed in force and actively administered, with implementing decrees still being consolidated, including a Landsbesluit under article 28(1) whose consolidated text was established on 7 May 2026 (P.B. 2026 no. 155). However the ordinance's own text is not published on the government law portal, so its provisions on registration, import, prescription status and penalties could not be verified.	Official
Iran	Grey Area	No	Not Scheduled	NAD+ supplements not specifically regulated. Supplement market exists but import restricted by sanctions. Domestic supplement production possible.	Secondary
Iraq	Grey Area	No	Not Scheduled	NAD+ supplements not specifically regulated. May enter through informal import channels.	Official
Lebanon	Grey Area	No	Not Scheduled	NAD+ supplements not specifically regulated. May be available through import or pharmacy channels. Crisis has created regulatory gaps.	Official
Montserrat	Grey Area	No	Not Within Scheduled Substances	No general medicines-approval law was located. Control rests on an Antibiotics and Therapeutic Substances Act of 1949-1951 vintage (Montserrat Cap. 14.14, Act 9 of 1950; Saint Kitts and Nevis Cap. 9.04) which requires an import licence, approved manufacturer and prescribed standards - but whose Schedule lists only penicillin, streptomycin, aureomycin, chloromycetin, sulphonamides, terramycin, bacitracin and neomycin. PEPTIDES ARE NOT WITHIN THAT SCHEDULE, so the import licence does not apply to them. In Turks and Caicos the position is similar: the Poisons Ordinance Cap. 8.05 requires a practitioner's written prescription for any declared poison, but its Schedule is a 1901-era list and does not include peptides; there is no medicines registration ordinance and no pharmacy ordinance. Penalties where the statutes do apply are negligible - EC$480 or six months in Montserrat, USD 5,000 in Turks and Caicos. The binding constraints for a novel non-scheduled substance in these jurisdictions are prescription-only supply, pharmacy and importer licensing, and customs, not medicines law.	Official
Pakistan	Grey Area	No	Not Scheduled	NAD+ supplements not specifically regulated by DRAP. Health supplements loosely controlled. May be available through import.	Official
Saba	Grey Area	No	Wet Geneesmiddelenvoorziening Bes	Bonaire, Sint Eustatius and Saba are Dutch public bodies, but the Dutch Geneesmiddelenwet does NOT extend to them - the applicable statute is the separate Wet op de geneesmiddelenvoorziening BES, cited by article in Staatscourant 2025 nr. 28064. Enforcement sits with the Dutch health inspectorate (IGJ) and the Minister of VWS. An adviescommissie geneesmiddelenvoorziening BES was established on 4 August 2025, but its remit is pharmacy establishment licensing, not product approval. No BES medicines-registration provision was located, so registration status, import rules, traveller allowance and penalties remain unverified for these islands.	Official
Saudi Arabia	Grey Area	No	Supplement (Unclear)	Supplement status uncertain under SFDA.	Official
Sint Eustatius	Grey Area	No	Wet Geneesmiddelenvoorziening Bes	Bonaire, Sint Eustatius and Saba are Dutch public bodies, but the Dutch Geneesmiddelenwet does NOT extend to them - the applicable statute is the separate Wet op de geneesmiddelenvoorziening BES, cited by article in Staatscourant 2025 nr. 28064. Enforcement sits with the Dutch health inspectorate (IGJ) and the Minister of VWS. An adviescommissie geneesmiddelenvoorziening BES was established on 4 August 2025, but its remit is pharmacy establishment licensing, not product approval. No BES medicines-registration provision was located, so registration status, import rules, traveller allowance and penalties remain unverified for these islands.	Official
St Kitts and Nevis	Grey Area	No	Not Within Scheduled Substances	No general medicines-approval law was located. Control rests on an Antibiotics and Therapeutic Substances Act of 1949-1951 vintage (Montserrat Cap. 14.14, Act 9 of 1950; Saint Kitts and Nevis Cap. 9.04) which requires an import licence, approved manufacturer and prescribed standards - but whose Schedule lists only penicillin, streptomycin, aureomycin, chloromycetin, sulphonamides, terramycin, bacitracin and neomycin. PEPTIDES ARE NOT WITHIN THAT SCHEDULE, so the import licence does not apply to them. In Turks and Caicos the position is similar: the Poisons Ordinance Cap. 8.05 requires a practitioner's written prescription for any declared poison, but its Schedule is a 1901-era list and does not include peptides; there is no medicines registration ordinance and no pharmacy ordinance. Penalties where the statutes do apply are negligible - EC$480 or six months in Montserrat, USD 5,000 in Turks and Caicos. The binding constraints for a novel non-scheduled substance in these jurisdictions are prescription-only supply, pharmacy and importer licensing, and customs, not medicines law.	Official
Turks and Caicos	Grey Area	No	Not Within Scheduled Substances	No general medicines-approval law was located. Control rests on an Antibiotics and Therapeutic Substances Act of 1949-1951 vintage (Montserrat Cap. 14.14, Act 9 of 1950; Saint Kitts and Nevis Cap. 9.04) which requires an import licence, approved manufacturer and prescribed standards - but whose Schedule lists only penicillin, streptomycin, aureomycin, chloromycetin, sulphonamides, terramycin, bacitracin and neomycin. PEPTIDES ARE NOT WITHIN THAT SCHEDULE, so the import licence does not apply to them. In Turks and Caicos the position is similar: the Poisons Ordinance Cap. 8.05 requires a practitioner's written prescription for any declared poison, but its Schedule is a 1901-era list and does not include peptides; there is no medicines registration ordinance and no pharmacy ordinance. Penalties where the statutes do apply are negligible - EC$480 or six months in Montserrat, USD 5,000 in Turks and Caicos. The binding constraints for a novel non-scheduled substance in these jurisdictions are prescription-only supply, pharmacy and importer licensing, and customs, not medicines law.	Official
Zimbabwe	Grey Area	No	Unregistered Medicine	Regulated by MCAZ under the Medicines and Allied Substances Control Act [Chapter 15:03]. Selling an unregistered "specified medicine" is an offence under s.29(1), penalty under s.29(1a): a fine not exceeding level twelve or imprisonment not exceeding 2 years, or both. The registration duty attaches only once the Minister has declared a medicine or class to be "specified" by statutory instrument under s.28. The Minister may separately prohibit or control manufacture, possession, sale or use of any medicine under s.38(1), same penalty. Notably, personal importation sits OUTSIDE the permit regime: SI 57 of 2008 s.3(d) disapplies the Import and Export of Medicines Regulations entirely to medicines imported by an individual for personal use. Access to unregistered medicines for a named person runs through the s.75 exemption power.	Official
Aruba	Prescription	No	Landsverordening Geneesmiddelenvoorziening	Regulated by the Inspectie Volksgezondheid Aruba (IVA) under the Landsverordening op de Geneesmiddelenvoorziening. Aruba is an autonomous country - Dutch and EU medicines law do NOT apply. Commercial importers and pharmacies must submit a sample to IVA for evaluation and classification before a product is placed on the market, and a GMP certificate is required where the product originates outside Europe, the USA or Canada. Personal importation is expressly quantified under IVA policy: prescription medicines up to 3 months' supply, supplements up to 3 months, non-prescription medicines up to 6 months, requiring customs documentation, ID, a photo of the package, and for prescription products a signed prescription from an authorised foreign doctor dated no more than 7 days before return. Critically for peptides: INJECTABLE AND INFUSION MEDICINES REQUIRE AN AUTHORISATION LETTER FROM AN ARUBA-BASED DOCTOR plus patient medical history. Courier companies must supply documentation to IVA.	Official
Cuba	Prescription	No	State System	State healthcare system only.	Unofficial
United Arab Emirates	Prescription	Yes	Clinic Prescribed	IV NAD+ available at wellness clinics. Must be clinic-administered.	Official
Belize	Banned	No	Unregistered No Product Licence	Not registered. Food and Drugs Act, Cap. 291, and the Food and Drugs (Registration, Licensing and Inspection) Regulations, S.I. 54 of 2017 (in force 29 July 2017; amended by S.I. 41 of 2021 and S.I. 136 of 2025). Regulation 3(1): a person shall not commercialise any drug unless they have obtained registration of, and received a product licence for, that drug from the competent authority - the Director of Health Services. Penalty under reg. 3(3): a fine up to BZD 10,000 on summary conviction. Registration requires a GMP certificate, a WHO-model Certificate of Pharmaceutical Product or Certificate of Free Sale, a certificate of analysis and a full technical dossier. The only non-registered import route is the orphan-drug pathway in reg. 5, which requires import authorisation and applies to drugs for rare diseases - a research peptide would not qualify. No personal or traveller allowance was located.	Official
Bolivia	Banned	No	Sin Registro Sanitario	No registro sanitario. Ley 1737 del Medicamento (17 December 1996) art. 5 subjects the elaboration, manufacture, distribution, import, export, sale and commercialisation of medicines to mandatory sanitary registration, restricts importation to persons with registered legal representation, and requires a certificate of registration for customs clearance. Art. 59 lists production, importation and commercialisation of medicines without registro sanitario as punishable infractions, and art. 61 provides for administrative sanctions plus criminal and civil liability under the relevant codes. The law contains no personal-use exception; any such exception would sit in the reglamento (D.S. 25235), which was not retrievable. AGEMED has issued NO alert naming research peptides - all 207 of its 2026 alerts were checked. Its 2026 peptide-adjacent activity concerns contraband tirzepatide and cosmetic products only. Tirzepatide IS legally registered in Bolivia, marketed by IMFAR S.R.L.	Official
Botswana	Banned	No	Unregistered Regulated Product	Regulated by BoMRA. A new Medicines and Related Substances Act 2025 (No. 29 of 2025) was assented on 24 December 2025 but COMMENCES ON NOTICE, and no commencement order was located - until it commences the 2013 Act continues to operate, so verify which regime applies before relying on this. Under the 2025 Act, s.35(1) prohibits possessing or controlling any regulated product for the purposes of importing, manufacturing, distributing, selling, advertising, STORING or dispensing unless registered - a possession-for-purpose offence, broader than a pure sale prohibition. Penalty under s.35(11): a fine up to P10,000,000 or imprisonment up to 10 YEARS, or both. Personal use is addressed: s.35(5)(a) allows exemption for a product prescribed outside Botswana for a patient's personal use, and s.64 permits a traveller to bring in quantities required for their own or accompanying family members' treatment, excluding prohibited products, narcotics, psychotropics and precursors.	Official
Cameroon	Banned	No	Sans Amm	No AMM. Loi n. 90/035 du 10 aout 1990 art. 64 prohibits supplying any pharmaceutical speciality, free or for payment, without the prior visa of the public health authority; Decret n. 98-405/PM du 22 octobre 1998 art. 3 subjects market placement to an AMM issued after homologation. Regulator is the DPML, a directorate of the Ministry of Public Health rather than an independent agency. The only route for non-homologated medicines is art. 34 of the 1998 decree, which permits import and use for therapeutic trial purposes by approved experts - there is no general named-patient or personal-import provision on the face of the instruments. Penalty exposure turns sharply on classification: breach of the visa requirement attracts only a fine (art. 66 applying art. 20, 50,000-500,000 FCFA), but any breach of the rules on importation, sale or use of substances veneneuses attracts art. 68 - a fine of 1,000,000-5,000,000 FCFA AND imprisonment of 1 to 10 years. Art. 69 extends the same penalties to possession without legitimate reason.	Official
Costa Rica	Banned	No	Sin Registro Sanitario	No registro sanitario. The Ministerio de Salud states that Ley General de Salud 5395 prohibits the importation, manufacture, commercialisation and use of products without sanitary registration, and that those involved face closure of their establishment and both administrative AND criminal sanctions. Advertencia Sanitaria 11-2026 (22 July 2026) names retatrutide, tesamorelin, BPC-157, TB-500 and GHK-Cu as promoted and sold through unauthorised channels without sanitary authorisation; MK-677 was named separately in Advertencia 14 (22 August 2025). Magistral preparation is not a route: the Ministry states such preparations may only be made by authorised pharmacies for a specific patient against an individual prescription, and may not be manufactured to hold inventory, sold at scale, or promoted publicly as substitutes for industrial medicines. Registered and prescription-only in Costa Rica: Ozempic (semaglutide), Saxenda (liraglutide) and Mounjaro KwikPen (tirzepatide).	Official
Guyana	Banned	No	New Drug Licence Required	Controlled through a "new drug" licence rather than a registry. Food and Drugs Act, Chapter 34:03 (Act 12 of 1971), Regulation 78(1): no person shall import, sell or advertise for sale a new drug unless they hold a licence in force issued by the Minister and have paid the licence fee. The definition of "new drug" captures every compound here - it includes any drug containing a substance not imported into Guyana for use as a drug before 1 January 1977, so all of these post-1977 compounds require a Ministerial licence to import or sell. At the border, s.22 allows an inspector to examine customs entries and take samples, and goods are not released until the analyst reports; where sale would contravene the Act the article is not admitted into Guyana. No personal-use exemption appears in the Act or Regulations. Penalties under s.33: on summary conviction GYD 6,500-32,500 and 1-3 months imprisonment for a first offence, rising to GYD 65,000-325,000 and 1-3 years on indictment, with forfeiture of the articles involved.	Official
Paraguay	Banned	No	Sin Registro Sanitario	No registro sanitario. Ley 1119/97 art. 6.1 prohibits commercialising or supplying free of charge any unregistered pharmaceutical speciality; art. 4.4 expressly prohibits sale of unauthorised or illegally introduced products. DINAVISA has issued three 2026 alerts naming these compounds: Alerta 05/2026 (3 March, Categoria A - Riesgo Grave) covering TB-500, BPC-157, CJC-1295 DAC, GHK-Cu, kisspeptin, PEG-MGF, SEMAX, tesamorelin and selank; Alerta 08/2026 (18 May) covering CJC-1295 + ipamorelin, TB-500, PT-141 and retatrutide; and Alerta 09/2026 (20 May) covering tirzepatide. NOTE A REGIONAL EXCEPTION: unlike its neighbours, Paraguay's art. 6.2 exempts medicines for personal use carried into the country by the user or an authorised third party, in strictly necessary and reasonable quantities, from prior authorisation - with no statutory condition of foreign approval and no prescription requirement. That exemption is worded for goods carried in person rather than posted, and DINAVISA enforces against unregistered peptide imports regardless.	Official
Senegal	Banned	No	Sans Amm	No marketing authorisation. Loi n. 2023-06 du 13 juin 2023 art. 133: no medicine may be supplied in Senegal, free of charge or for payment, without first obtaining an AMM granted by order of the Minister of Health. Import is closed to the general public - art. 136 restricts it to authorised manufacturing and wholesale establishments, and art. 137 requires an ARP authorisation for every import. Personal importation is available only exceptionally: art. 141 permits import authorisations to be granted to private individuals on conditions set by decree, and the implementing decree was not located. Penalties are severe: art. 209 punishes supplying, storing, distributing or selling medicines OUTSIDE health establishments and the official circuit with 5 to 10 YEARS imprisonment and a fine of 500,000 to 10,000,000 FCFA. Illegal practice of pharmacy (art. 203) carries the same custodial range.	Official
Trinidad and Tobago	Banned	No	New Drug Approval Required	Food and Drugs Act, Chap. 30:01 and the Food and Drugs Regulations operate a genuine new-drug approval regime. Second Schedule, Division 3, para. 2(1): no person shall import, sell or advertise for sale a new drug unless a new drug submission has been filed, the fee paid, and the Minister has issued a notice of approval that has not been withdrawn. "New drug" captures any substance not imported into Trinidad and Tobago as a drug before the appointed day, which takes in modern peptides. A narrow research carve-out exists at Division 3, para. 10 - import for qualified investigators solely to obtain clinical and scientific data, labelled "To Be Used By Qualified Investigators Only" and requiring written ministerial authority naming them. Section 32(2) additionally bars import unless the article wholly conforms to the law of the country of manufacture and is accompanied by a certificate that its sale there would not violate that law - which defeats import of anything sold abroad as a research chemical not for human consumption. Third Schedule drugs are prescription-only, though a resident of a foreign country visiting Trinidad and Tobago is exempt from the import restriction. Penalties (s.33): summary first offence TTD 1,500 and 3 months; on indictment TTD 15,000 and 3 years.	Official
Uruguay	Banned	No	No Registrado	Not registered with the MSP. Decreto 521/984 art. 119 requires every medicine to be registered before use or commercialisation, and art. 82 prohibits the export, import and commercialisation of unregistered human medicines. Personal importation confers no right: art. 73 provides that the introduction or removal of human medicines by private individuals without complying with the requirements triggers MSP intervention over the final destination of the products. Only two routes exist for an unregistered medicine and neither is open to research peptides - art. 71 (samples of new medicines solely for clinical experimentation under MSP control or for the registration process) and art. 143 (urgency or emergency, requiring a competent professional's request and DI.QUI.ME. authorisation, with the professional and supplier jointly and severally liable). Penalties under Decreto-Ley 15.443 art. 19: closure of the establishment, seizure of goods and fines, updated annually for cost of living.	Official
Venezuela	Banned	No	No Registrado	Not registered. Ley de Medicamentos (Gaceta Oficial 37.006, 3 August 2000) art. 18 requires registration before elaboration, distribution, POSSESSION (tenencia), sale or dispensing - note that the article reaches mere possession, which is unusual. Art. 58 prohibits the sale of medicines not registered in the country, and art. 67 flatly prohibits importing medicines that do not meet the requirements of the legislation, the only carve-out being for the National Executive during a declared health emergency. The law contains no personal-use or traveller exception. Penalties: art. 75(1) treats manufacture, import, export and distribution of medicines without authorisation as an administrative offence fined 185-370 tax units; criminal liability arises under art. 77 (6 months to 2 years for dispensing non-compliant medicines endangering health) and art. 78 (6 months to 3 years for altering composition, imitating medicines, or stocking, advertising, offering or selling a product known to be altered).	Official
Vietnam	Banned	No	Unregistered Unauthorised	Not authorised for circulation. Pharmacy Law 105/2016/QH13 art. 6(5)(e) strictly prohibits trading in drugs or drug substances not yet permitted for circulation; art. 59(1) limits the market to drugs holding a marketing authorisation or imported under art. 60. Unregistered drugs may be import-licensed only in enumerated cases under art. 60(2), of which limb (i) covers non-commercial purposes. Criminal exposure runs through Penal Code art. 194 (counterfeit medicines): 2-7 years base, rising to 12-20 years or life in aggravated cases. IMPORTANT: the death penalty was REMOVED from art. 194 with effect from 1 July 2025 by Law 86/2025/QH15 - older sources stating otherwise are out of date. Note art. 194 targets counterfeit rather than merely unregistered product, though Vietnam's definition of counterfeit captures goods with absent or deficient active ingredient. Semaglutide and tirzepatide are prescription-only by residual rule: anything not on the OTC list in Circular 07/2017/TT-BYT is automatically a prescription drug.	Official
Zambia	Banned	No	Unregistered Medicine	Not registered with ZAMRA. Medicines and Allied Substances Act 2013 (Act No. 3 of 2013) s.39(1) prohibits placing a medicine on the market without a marketing authorisation. Dealing in unregistered medicines is a distinct and more serious offence under s.58(2)(a): a fine up to 4,000,000 penalty units or imprisonment up to 7 YEARS, or both, plus forfeiture and licence cancellation. Importing without a permit is a further offence under s.35 (up to 3 years). Personal importation is permitted narrowly: s.39(4)(b) exempts a person importing for their own or a relative's use ONLY where the quantity is based on a prescription. A traveller carve-out exists at s.35(2) but the quantity is set by statutory instrument which was not located.	Official

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Entries marked Official cite a government regulator, legislation or an official gazette. Entries marked Secondary rest on consultancy, law firm, news or academic reporting rather than the regulator itself. Entries marked Unofficial rest on sources that are not authoritative — which may include commercial sellers, medicine-import services or independent websites. Some entries currently carry no source at all.

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Data is researcher-verified but not legal advice. Regulations change frequently. Always verify with local authorities before purchasing, importing, or traveling with peptides. Last verified: 2026-02-28.