FDA NDC Directory · JSON-LD · Markdown

Nicardipine Hydrochloride

NDC 70069-875 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerSomerset Therapeutics, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA220243
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsNICARDIPINE HYDROCHLORIDE (.1 mg/mL)
Marketing started20260420
Package count1

External sources

Source: openFDA. Public-domain (CC0).