FDA NDC Directory · JSON-LD · Markdown

Nicardipine Hydrochloride

NDC 70710-2011 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218638
Dosage form / routeCAPSULE · ORAL
Active ingredientsNICARDIPINE HYDROCHLORIDE (30 mg/1)
Marketing started20250801
Package count1

External sources

Source: openFDA. Public-domain (CC0).