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DOPAMINE HYDROCHLORIDE

NDC 51662-1489 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryAbbreviated NDA (generic) · App ANDA207707
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsDOPAMINE HYDROCHLORIDE (40 mg/mL)
Marketing started20210807
Package count2

External sources

Source: openFDA. Public-domain (CC0).