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Nalbuphine Hydrochloride

NDC 0409-1465 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameNALBUPHINE HYDROCHLORIDE
Labeler / ManufacturerHospira, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA070916
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALBUPHINE HYDROCHLORIDE (20 mg/mL)
Marketing started20041231
Package count1

External sources

Source: openFDA. Public-domain (CC0).