"65597-118-07" National Drug Code (NDC)

NDC Code	65597-118-07
Package Description	7 TABLET, FILM COATED in 1 BOTTLE (65597-118-07)
Product NDC	65597-118
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tribenzor
Non-Proprietary Name	Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20100731
End Marketing Date	20240229
Marketing Category Name	NDA
Application Number	NDA200175
Manufacturer	Daiichi Sankyo, Inc.
Substance Name	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength	10; 25; 40
Strength Unit	mg/1; 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], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]