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EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE

NDC 69097-741 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090958
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsEMTRICITABINE (200 mg/1)
TENOFOVIR DISOPROXIL FUMARATE (300 mg/1)
Marketing started20211101
Package count1

External sources

Source: openFDA. Public-domain (CC0).