"70518-4165-0" National Drug Code (NDC)

NDC Code	70518-4165-0
Package Description	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4165-0)
Product NDC	70518-4165
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Non-Proprietary Name	Olmesartan Medoxomil / Amlodipine Besylate / Hydrochlorothiazide
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20240822
Marketing Category Name	ANDA
Application Number	ANDA206137
Manufacturer	REMEDYREPACK INC.
Substance Name	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength	5; 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]