"70518-3657-0" National Drug Code (NDC)

NDC Code	70518-3657-0
Package Description	90 CAPSULE in 1 BOTTLE, PLASTIC (70518-3657-0)
Product NDC	70518-3657
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Benazepril Hydrochloride
Non-Proprietary Name	Amlodipine And Benazepril Hydrochloride
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20230222
Marketing Category Name	ANDA
Application Number	ANDA202239
Manufacturer	REMEDYREPACK INC.
Substance Name	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE
Strength	10; 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]