"69452-436-19" National Drug Code (NDC)

NDC Code	69452-436-19
Package Description	90 CAPSULE in 1 BOTTLE, PLASTIC (69452-436-19)
Product NDC	69452-436
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Nicardipine Hydrochloride
Non-Proprietary Name	Nicardipine Hydrochloride
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20241104
Marketing Category Name	ANDA
Application Number	ANDA217555
Manufacturer	Bionpharma Inc.
Substance Name	NICARDIPINE HYDROCHLORIDE
Strength	20
Strength Unit	mg/1
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]