"72162-2379-3" National Drug Code (NDC)

NDC Code	72162-2379-3
Package Description	30 TABLET in 1 BOTTLE (72162-2379-3)
Product NDC	72162-2379
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine And Olmesartan Medoxomil
Non-Proprietary Name	Amlodipine And Olmesartan Medoxomil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20180101
Marketing Category Name	ANDA
Application Number	ANDA207435
Manufacturer	Bryant Ranch Prepack
Substance Name	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength	5; 20
Strength Unit	mg/1; mg/1
Pharmacy Classes	Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS]