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OxyContin

NDC 59011-415 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameoxycodone hydrochloride
Labeler / ManufacturerKnoa Pharma LLC
Marketing categoryNew Drug Application (innovator) · App NDA022272
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsOXYCODONE HYDROCHLORIDE (15 mg/1)
Marketing started20100808
Package count2

External sources

Source: openFDA. Public-domain (CC0).