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LAMIVUDINE AND ZIDOVUDINE

NDC 72865-144 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namelamivudine and zidovudine
Labeler / ManufacturerXLCare Pharmaceuticals, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA203259
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (150 mg/1)
ZIDOVUDINE (300 mg/1)
Marketing started20200417
Package count1

External sources

Source: openFDA. Public-domain (CC0).