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hydrALAZINE Hydrochloride

NDC 70518-3659 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA040388
Dosage form / routeINJECTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsHYDRALAZINE HYDROCHLORIDE (20 mg/mL)
Marketing started20230227
Package count1

External sources

Source: openFDA. Public-domain (CC0).