"63629-1454-1" National Drug Code (NDC)

NDC Code	63629-1454-1
Package Description	30 CAPSULE in 1 BOTTLE (63629-1454-1)
Product NDC	63629-1454
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine Besylate And Benazepril Hydrochloride
Non-Proprietary Name	Amlodipine Besylate And Benazepril Hydrochloride
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20100419
Marketing Category Name	ANDA
Application Number	ANDA077183
Manufacturer	Bryant Ranch Prepack
Substance Name	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength	5; 20
Strength Unit	mg/1; mg/1
Pharmacy Classes	Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]