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Nicardipine Hydrochloride

NDC 24658-751 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerPuraCap Laboratories LLC dba Blu Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA074928
Dosage form / routeCAPSULE · ORAL
Active ingredientsNICARDIPINE HYDROCHLORIDE (30 mg/1)
Marketing started20161215
Package count1

External sources

Source: openFDA. Public-domain (CC0).