FDA NDC Directory · JSON-LD · Markdown

OXYCODONE HYDROCHLORIDE

NDC 67296-0425 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameoxycodone hydrochloride
Labeler / ManufacturerRedPharm Drug, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076758
Dosage form / routeTABLET · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20090730
Package count2

External sources

Source: openFDA. Public-domain (CC0).