FDA NDC Directory · JSON-LD · Markdown

Abacavir

NDC 68084-021 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA077844
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABACAVIR SULFATE (300 mg/1)
Marketing started20130204
Package count1

External sources

Source: openFDA. Public-domain (CC0).