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Nalbuphine hydrochloride

NDC 71872-7331 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMedical Purchasing Solutions, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA216049
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active ingredientsNALBUPHINE HYDROCHLORIDE (10 mg/mL)
Marketing started20240926
Package count1

External sources

Source: openFDA. Public-domain (CC0).