"50090-5357-0" National Drug Code (NDC)

NDC Code	50090-5357-0
Package Description	90 CAPSULE in 1 BOTTLE (50090-5357-0)
Product NDC	50090-5357
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	20110705
Marketing Category Name	ANDA
Application Number	ANDA078466
Manufacturer	A-S Medication Solutions
Substance Name	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength	5; 40
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]