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hydrALAZINE Hydrochloride

NDC 63323-614 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA040388
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsHYDRALAZINE HYDROCHLORIDE (20 mg/mL)
Marketing started20110131
Package count1

External sources

Source: openFDA. Public-domain (CC0).