NDC 0517-0735 – Nicardipine Hydrochloride

Nicardipine Hydrochloride 2.5 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0517-0735

Product details

Brand name
Nicardipine Hydrochloride
Generic name
Nicardipine hydrochloride
Labeler
American Regent, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA090534
Marketed since
May 8, 2020
Listing expires
December 31, 2026
Pharmacologic class
Dihydropyridine Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Nicardipine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
0517-0735-1010 VIAL in 1 CARTON (0517-0735-10) / 10 mL in 1 VIAL (0517-0735-01)May 8, 2020

Recalls mentioning this NDC

Other Nicardipine Hydrochloride products