FDA NDC Directory · JSON-LD · Markdown

Oxycodone Hydrochloride

NDC 0904-6966 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameOxycodone
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA203638
Dosage form / routeTABLET · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (5 mg/1)
Marketing started20121030
Package count1

External sources

Source: openFDA. Public-domain (CC0).