FDA NDC Directory · JSON-LD · Markdown

Abacavir

NDC 69097-514 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCipla USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078119
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABACAVIR SULFATE (300 mg/1)
Marketing started20171121
Package count1

External sources

Source: openFDA. Public-domain (CC0).