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Emtricitabine and tenofovir disoproxil fumarate

NDC 82804-086 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA201806
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsEMTRICITABINE (200 mg/1)
TENOFOVIR DISOPROXIL FUMARATE (300 mg/1)
Marketing started20211007
Package count2

External sources

Source: openFDA. Public-domain (CC0).