FDA NDC Directory · JSON-LD · Markdown

Nicardipine hydrochloride

NDC 69238-2691 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic nameNicardipine
Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218202
Dosage form / routeCAPSULE · ORAL
Active ingredientsNICARDIPINE HYDROCHLORIDE (20 mg/1)
Marketing started20241003
Package count1

External sources

Source: openFDA. Public-domain (CC0).