FDA NDC Directory · JSON-LD · Markdown

OXYMORPHONE HYDROCHLORIDE

NDC 72865-130 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerXLCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210175
Dosage form / routeTABLET · ORAL
Active ingredientsOXYMORPHONE HYDROCHLORIDE (5 mg/1)
Marketing started20200506
Package count1

External sources

Source: openFDA. Public-domain (CC0).