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Nicardipine Hydrochloride

NDC 65219-298 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerFresenius Kabi USA, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA219334
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsNICARDIPINE HYDROCHLORIDE (.2 mg/mL)
Marketing started20261001
Package count1

External sources

Source: openFDA. Public-domain (CC0).