"0517-0735-10" National Drug Code (NDC)

NDC Code	0517-0735-10
Package Description	10 VIAL in 1 CARTON (0517-0735-10) > 10 mL in 1 VIAL (0517-0735-01)
Product NDC	0517-0735
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nicardipine Hydrochloride
Non-Proprietary Name	Nicardipine Hydrochloride
Dosage Form	INJECTION, SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20200508
Marketing Category Name	ANDA
Application Number	ANDA090534
Manufacturer	American Regent, Inc.
Substance Name	NICARDIPINE HYDROCHLORIDE
Strength	2.5
Strength Unit	mg/mL
Pharmacy Classes	Calcium Channel Antagonists [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]