FDA NDC Directory · JSON-LD · Markdown

Hydromorphone Hydrochloride

NDC 60687-579 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA076855
Dosage form / routeTABLET · ORAL
Active ingredientsHYDROMORPHONE HYDROCHLORIDE (2 mg/1)
Marketing started20210511
Package count1

External sources

Source: openFDA. Public-domain (CC0).