Regulatory PathRegulatory requirements compared

Active substance

Tenofovir

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
Disoten245 mgFilm-coated tablet · Oral use30 BottleSAR 723.25Generic · PrescriptionTabuk Pharmaceutical Manufacturing CompanyValid
Hivera300 mgFilm-coated tablet · Oral use30 BottleSAR 783.65Generic · PrescriptionMed City PharmaValid
TENOVAS245 mgFilm-coated tablet · Oral use30 BlisterSAR 744.45Generic · PrescriptionAlrai Pharmaceutical industry Co. (L.L.C)Valid
Tenovas245 mgFilm-coated tablet · Oral use30 BottleSAR 744.45Generic · PrescriptionAlrai Pharmaceutical industry Co. (L.L.C)Valid
VEMLIDY 25MG F.C.TABLET25 mgFilm-coated tablet · Oral use30 BottleSAR 940.90NCE · PrescriptionGilead Sciences International LtdValid
VIRLAIO245 mgFilm-coated tablet · Oral use30 BlisterSAR 723.25Generic · PrescriptionALPHA PHARMA INDUSTRYValid
Virad300 mgFilm-coated tablet · Oral use30 BlisterSAR 843.90Generic · PrescriptionSaudi AmaroxValid
VIREAD 245 mg FILM COATED TABLET245 mgFilm-coated tablet · Oral use30 BottleSAR 904.20NCE · PrescriptionGlaxo Saudi Arabia LtdWithdrawn by MAH · Not Marketed
Indications — CHI Daman Drug Formulary

ANTIMICROBIAL PROPHYLAXIS IN CANCER PATIENTS; BURKITT`S LYMPHOMA-HBV PROPHYLAXIS; CHRONIC LYMPHOCYTIC LEUKEMIA (CLL)-HBV PROPHYLAXIS; DIFFUSE LARGE B-CELL LYMPHOMA (DLBCL)-HBV PROPHYLAXIS; FOLLICULAR LYMPHOMA-HBV PROPHYLAXIS; HEPATITIS B; HODGKIN'S LYMPHOMA-HBV PROPHYLAXIS; HUMAN IMMUNODEFICIENCY VIRUS; MANTLE CELL LYMPHOMA-HBV PROPHYLAXIS; MARGINAL ZONE LYMPHOMA-HBV PROPHYLAXIS; PEDIATRIC B-CELL LYMPHOMA-HBV PROPHYLAXIS

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
VIREAD300MG; 150MG; 200MG; 250MGtablet · oralGILEAD SCIENCES INCPrescription26 Oct 2001
VIREAD40MG/SCOOPFULpowder · oralGILEAD SCIENCES INCPrescription18 Jan 2012
TENOFOVIR DISOPROXIL FUMARATE300MG; 150MG; 200MG; 250MGtablet · oralTEVA PHARMS USAPrescription18 Mar 2015
VEMLIDYEQ 25MG BASEtablet · oralGILEAD SCIENCES INCPrescription10 Nov 2016
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralCIPLAPrescription26 Jan 2018
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralHETERO LABS LTD IIIPrescription26 Jan 2018
TENOFOVIR DISOPROXIL FUMARATE150MG; 200MG; 250MG; 300MGtablet · oralAUROBINDO PHARMAPrescription26 Jan 2018
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralSTRIDES PHARMAPrescription26 Jan 2018
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralMACLEODS PHARMSPrescription26 Jan 2018
TENOFOVIR DISOPROXIL FUMARATE200MG; 250MG; 300MGtablet · oralQILUPrescription2 Mar 2018
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralCHARTWELLPrescription31 Jul 2018
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralREYOUNGPrescription2 Mar 2023
TENOFOVIR ALAFENAMIDEEQ 25MG BASEtablet · oralLUPINPrescription30 Mar 2023
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralPHARMOBEDIENTPrescription29 Feb 2024
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralMICRO LABSPrescription18 Dec 2025
TENOFOVIR DISOPROXIL FUMARATE300MGtablet · oralCHARTWELL RXDiscontinued26 Feb 2018
TENOFOVIR DISOPROXIL FUMARATE150MG; 200MG; 250MG; 300MGtablet · oralPHARMOBEDIENTDiscontinued27 Nov 2018
TENOFOVIR ALAFENAMIDE FUMARATEEQ 25MG BASEtablet · oralAPOTEXDiscontinued21 Mar 2024

EMA European Union — centrally authorised medicines

Viread Gilead Sciences Ireland UC · Authorised · authorised 4 Feb 2002 · ATC J05AF07

Therapeutic indication (EMA)

HIV 1 infection Viread 123 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, aged 6 to < 12 years who weigh from 17 kg to less than 22 kg. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 123 mg film coated tablets are indicated for the treatment of chronic hepatitis B in paediatric patients aged 6 to < 12 years who weigh from 17 kg to less than 22 kg, with compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis. With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 163 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, aged 6 to < 12 years who weigh from 22 kg to less than 28 kg. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 163 mg film coated tablets are indicated for the treatment of chronic hepatitis B in paediatric patients aged 6 to < 12 years who weigh from 22 kg to less than 28 kg, with: compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis. With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 204 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, aged 6 to < 12 years who weigh from 28 kg to less than 35 kg. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 204 mg film coated tablets are indicated for the treatment of chronic hepatitis B in paediatric patients aged 6 to < 12 years who weigh from 28 kg to less than 35 kg, with: compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels or histological evidence of moderate to severe inflammation and/or fibrosis. With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 245 mg film coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected adults. In adults, the demonstration of the benefit of Viread in HIV 1 infection is based on results of one study in treatment naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which Viread was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). Viread 245 mg film coated tablets are also indicated for the treatment of HIV 1 infected adolescents, with NRTI resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years. The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 245 mg film coated tablets are indicated for the treatment of chronic hepatitis B in adults with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis (see section 5.1). evidence of lamivudine resistant hepatitis B virus (see sections 4.8 and 5.1). decompensated liver disease (see sections 4.4, 4.8 and 5.1). Viread 245 mg film coated tablets are indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with: compensated liver disease and evidence of immune active disease, i.e. active viral replication and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis. With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1. HIV 1 infection Viread 33 mg/g granules are indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected paediatric patients, with NRTI resistance or toxicities precluding the use of first line agents, from 2 to < 6 years of age, and above 6 years of age for whom a solid dosage form is not appropriate. Viread 33 mg/g granules are also indicated in combination with other antiretroviral medicinal products for the treatment of HIV 1 infected adults for whom a solid dosage form is not appropriate. In adults, the demonstration of the benefit of Viread in HIV 1 infection is based on results of one study in treatment naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which Viread was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). The choice of Viread to treat antiretroviral experienced patients with HIV 1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Viread 33 mg/g granules are indicated for the treatment of chronic hepatitis B in adults for whom a solid dosage form is not appropriate with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis (see section 5.1). evidence of lamivudine resistant hepatitis B virus (see sections 4.8 and 5.1). decompensated liver disease (see sections 4.4, 4.8 and 5.1). Viread 33 mg/g granules are also indicated for the treatment of chronic hepatitis B in paediatric patients2 to < 18 years of age for whom a solid dosage form is not appropriate with: compensated liver disease and evidence of immune active disease, i.e. active viral replication, and persistently elevated serum ALT levels, or histological evidence of moderate to severe inflammation and/or fibrosis. With respect to the decision to initiate treatment in paediatric patients, see sections 4.2, 4.4, 4.8 and 5.1.

Tenofovir disoproxil Zentiva Zentiva k.s. · Authorised · authorised 15 Sep 2016 · ATC J05AF07

Therapeutic indication (EMA)

HIV?1 infection Tenofovir disoproxil Zentiva is indicated in combination with other antiretroviral medicinal products for the treatment of HIV?1 infected adults. In adults, the demonstration of the benefit of tenofovir disoproxil in HIV?1 infection is based on results of one study in treatment?naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which tenofovir disoproxil was added to stable background therapy (mainly tritherapy) in antiretroviral pre?treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). Tenofovir disoproxil Zentiva is also indicated for the treatment of HIV?1 infected adolescents, with NRTI (nucleotide reverse transcriptase inhibitor) resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years. The choice of Tenofovir disoproxil Zentiva to treat antiretroviral?experienced patients with HIV?1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Tenofovir disoproxil Zentiva is indicated for the treatment of chronic hepatitis B in adults with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis (see section 5.1); evidence of lamivudine-resistant hepatitis B virus (see sections 4.8 and 5.1); decompensated liver disease (see sections 4.4, 4.8 and 5.1). Tenofovir disoproxil Zentiva is indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with: compensated liver disease and evidence of immune active disease, i.e. active viral replication, persistently elevated serum ALT levels and histological evidence of active inflammation and/or fibrosis (see sections 4.4, 4.8 and 5.1).

Tenofovir disoproxil Viatris (previously Tenofovir disoproxil Mylan) Viatris Limited · Authorised · authorised 8 Dec 2016 · ATC J05AF07

Therapeutic indication (EMA)

HIV-1 infection Tenofovir disoproxil 245 mg film-coated tablets are indicated in combination with other antiretroviral medicinal products for the treatment of HIV-1 infected adults. In adults, the demonstration of the benefit of tenofovir disoproxil in HIV-1 infection is based on results of one study in treatment-naïve patients, including patients with a high viral load (> 100,000 copies/ml) and studies in which tenofovir disoproxil was added to stable background therapy (mainly tritherapy) in antiretroviral pre-treated patients experiencing early virological failure (< 10,000 copies/ml, with the majority of patients having < 5,000 copies/ml). Tenofovir disoproxil 245 mg film-coated tablets are also indicated for the treatment of HIV-1 infected adolescents, with NRTI resistance or toxicities precluding the use of first line agents, aged 12 to < 18 years. The choice of tenofovir disoproxil to treat antiretroviral-experienced patients with HIV-1 infection should be based on individual viral resistance testing and/or treatment history of patients. Hepatitis B infection Tenofovir disoproxil 245 mg film-coated tablets are indicated for the treatment of chronic hepatitis B in adults with: compensated liver disease, with evidence of active viral replication, persistently elevated serum alanine aminotransferase (ALT) levels and histological evidence of active inflammation and/or fibrosis. evidence of lamivudine-resistant hepatitis B virus. decompensated liver disease. Tenofovir disoproxil 245 mg film-coated tablets are indicated for the treatment of chronic hepatitis B in adolescents 12 to < 18 years of age with: compensated liver disease and evidence of immune active disease, i.e. active viral replication, persistently elevated serum ALT levels and histological evidence of active inflammation and/or fibrosis.

Vemlidy Gilead Sciences Ireland UC · Authorised · authorised 9 Jan 2017 · ATC J05AF13

Therapeutic indication (EMA)

Vemlidy is indicated for the treatment of chronic hepatitis B (CHB) in adults and paediatric patients 6 years of age and older weighing at least 25 kg (see section 5.1).

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
AG-TENOFOVIR02516276300 MGTABLET · ORALANGITA PHARMA INC.
APO-TENOFOVIR02451980300 MGTABLET · ORALAPOTEX INC
AURO-TENOFOVIR02460173300 MGTABLET · ORALAURO PHARMA INC
JAMP-TENOFOVIR02479087300 MGTABLET · ORALJAMP PHARMA CORPORATION
MINT-TENOFOVIR02512939300 MGTABLET · ORALMINT PHARMACEUTICALS INC
MYLAN-TENOFOVIR DISOPROXIL02452634300 MGTABLET · ORALMYLAN PHARMACEUTICALS ULC
NAT-TENOFOVIR02472511300 MGTABLET · ORALNATCO PHARMA (CANADA) INC
PMS-TENOFOVIR02453940300 MGTABLET · ORALPHARMASCIENCE INC
RIVA-TENOFOVIR02515156300 MGTABLET · ORALLABORATOIRE RIVA INC.
TENOFOVIR02512327300 MGTABLET · ORALSANIS HEALTH INC
TENOFOVIR02523922300 MGTABLET · ORALSIVEM PHARMACEUTICALS ULC
TEVA-TENOFOVIR02403889300 MGTABLET · ORALTEVA CANADA LIMITED
VEMLIDY0246424125 MGTABLET · ORALGILEAD SCIENCES CANADA INC
VIREAD02247128300 MGTABLET · ORALGILEAD SCIENCES CANADA INC

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACTENOFOVIR DISOPROXIL FUMARATE 300 MG TABLET$0.29381per EA23 Sep 2026
US NADACVEMLIDY 25 MG TABLET$51.98384per EA23 Sep 2026
US NADACVIREAD 300 MG TABLET$40.6865per EA23 Sep 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

WHO WHO Model List of Essential Medicines (2025)

  • 6.4.2.1. Antiretrovirals > Nucleoside/Nucleotide reverse transcriptase inhibitors · core
    Contact with or exposure to human immunodeficiency virus; Human immunodeficiency virus disease without mention of tuberculosis or malaria, clinical stage unspecified
    Oral > Solid: 300 mg tablet (equivalent to 245 mg tenofovir disoproxil)
  • 6.4.4.1.1. Medicines for hepatitis B > Nucleoside/Nucleotide reverse transcriptase inhibitors · core
    Chronic hepatitis B
    Oral > Solid: 300 mg tablet (equivalent to 245 mg tenofovir disoproxil)

Safety signals and safety-related labeling changes

  • US FDA 29 Sep 2026 DELSTRIGO — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 30 Jul 2025 BIKTARVY — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 20 Jun 2025 DESCOVY — safety-related labeling change
    Labeling sections changed: Boxed Warning; Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 19 Feb 2025 ODEFSEY — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 27 Mar 2024 VEMLIDY — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 31 Mar 2023 SYMTUZA — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 7 Jan 2022 GENVOYA — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 21 Aug 2020 STRIBILD — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 23 Jun 2020 TRUVADA — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 27 Nov 2019 COMPLERA — safety-related labeling change
    Labeling sections changed: Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 29 Oct 2019 ATRIPLA — safety-related labeling change
    Labeling sections changed: Boxed Warning; Contraindications; Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 29 Oct 2019 SYMFI — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 29 Oct 2019 SYMFI LO — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 29 Oct 2019 TEMIXYS — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide
  • US FDA 24 Apr 2019 VIREAD — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Adverse Reactions; Drug Interactions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide

All safety entries for tenofovir →

Combinations containing Tenofovir

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.