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Oxymorphone hydrochloride

NDC 0115-1233 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAmneal Pharmaceuticals of New York LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA079087
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsOXYMORPHONE HYDROCHLORIDE (20 mg/1)
Marketing started20130102
Package count4

External sources

Source: openFDA. Public-domain (CC0).