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Emtricitabine and tenofovir disoproxil fumarate

NDC 70771-1622 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA212689
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsEMTRICITABINE (167 mg/1)
TENOFOVIR DISOPROXIL FUMARATE (250 mg/1)
Marketing started20210701
Package count3

External sources

Source: openFDA. Public-domain (CC0).