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Lamivudine and Zidovudine

NDC 65862-036 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077558
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLAMIVUDINE (150 mg/1)
ZIDOVUDINE (300 mg/1)
Marketing started20170505
Package count2

External sources

Source: openFDA. Public-domain (CC0).