"0078-0406-05" National Drug Code (NDC)

NDC Code	0078-0406-05
Package Description	100 CAPSULE in 1 BOTTLE (0078-0406-05)
Product NDC	0078-0406
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lotrel
Non-Proprietary Name	Amlodipine Besylate And Benazepril Hydrochloride
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	19950303
End Marketing Date	20260930
Marketing Category Name	NDA
Application Number	NDA020364
Manufacturer	Novartis Pharmaceuticals Corporation
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]