"55154-9668-2" National Drug Code (NDC)

NDC Code	55154-9668-2
Package Description	1200 CAPSULE in 1 BOTTLE, PLASTIC (55154-9668-2)
Product NDC	55154-9668
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	Cardinal Health
Substance Name	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength	10; 40
Strength Unit	mg/1; mg/1
Pharmacy Classes	Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]