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NICARDIPINE HYDROCHLORIDE

NDC 65219-818 · HUMAN PRESCRIPTION DRUG · INJECTION

Generic nameNicardipine Hydrochloride
Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA217548
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsNICARDIPINE HYDROCHLORIDE (25 mg/10mL)
Marketing started20240911
Package count2

External sources

Source: openFDA. Public-domain (CC0).