FDA NDC Directory · JSON-LD · Markdown

OXYMORPHONE HYDROCHLORIDE

NDC 31722-929 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCamber Pharmaceuticals, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA210175
Dosage form / routeTABLET · ORAL
Active ingredientsOXYMORPHONE HYDROCHLORIDE (5 mg/1)
Marketing started20180301
Package count1

External sources

Source: openFDA. Public-domain (CC0).