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Abacavir and Lamivudine

NDC 42385-962 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerLaurus Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216332
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABACAVIR SULFATE (600 mg/1)
LAMIVUDINE (300 mg/1)
Marketing started20220725
Package count3

External sources

Source: openFDA. Public-domain (CC0).