"27241-086-03" National Drug Code (NDC)

NDC Code	27241-086-03
Package Description	30 TABLET in 1 BOTTLE (27241-086-03)
Product NDC	27241-086
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Amlodipine Besylate And Olmesartan Medoxomil
Non-Proprietary Name	Amlodipine Besylate And Olmesartan Medoxomil
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170206
Marketing Category Name	ANDA
Application Number	ANDA207216
Manufacturer	Ajanta Pharma USA Inc.
Substance Name	AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL
Strength	10; 40
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]