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Nicardipine Hydrochloride

NDC 67184-0611 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerQilu Pharmaceutical Co., Ltd.
Marketing categoryAbbreviated NDA (generic) · App ANDA219608
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsNICARDIPINE HYDROCHLORIDE (2.5 mg/mL)
Marketing started20251028
Package count1

External sources

Source: openFDA. Public-domain (CC0).