"71335-1946-1" National Drug Code (NDC)

NDC Code	71335-1946-1
Package Description	30 CAPSULE in 1 BOTTLE (71335-1946-1)
Product NDC	71335-1946
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	20180801
Marketing Category Name	ANDA
Application Number	ANDA078466
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]