NDC 0143-9689 – Nicardipine Hydrochloride

Nicardipine Hydrochloride 25 mg/10mL · Injection · Intravenous

Human Prescription Drug 1 recall

Product NDC0143-9689

Product details

Brand name
Nicardipine Hydrochloride
Generic name
Nicardipine Hydrochloride
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Injection
Route
Intravenous
Marketing category
NDA · NDA022276
Marketed since
March 2, 2012
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
0143-9689-1010 VIAL in 1 CARTON (0143-9689-10) / 10 mL in 1 VIAL (0143-9689-01)Mar 2, 2012

Recalls mentioning this NDC

Other Nicardipine Hydrochloride products