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Oxycodone Hydrochloride

NDC 65162-050 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameOxycodone
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203638
Dosage form / routeTABLET · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (20 mg/1)
Marketing started20121030
Package count3

External sources

Source: openFDA. Public-domain (CC0).