"55289-096-30" National Drug Code (NDC)

NDC Code	55289-096-30
Package Description	30 CAPSULE in 1 BOTTLE, PLASTIC (55289-096-30)
Product NDC	55289-096
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
Marketing Category Name	NDA
Application Number	NDA020364
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength	5; 10
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]