FDA NDC Directory · JSON-LD · Markdown

Hydromorphone Hydrochloride

NDC 0641-6169 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216899
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsHYDROMORPHONE HYDROCHLORIDE (1 mg/mL)
Marketing started20240426
Package count1

External sources

Source: openFDA. Public-domain (CC0).