"42571-245-05" National Drug Code (NDC)

NDC Code	42571-245-05
Package Description	500 TABLET, FILM COATED in 1 BOTTLE (42571-245-05)
Product NDC	42571-245
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
Non-Proprietary Name	Olmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20260301
Marketing Category Name	ANDA
Application Number	ANDA207437
Manufacturer	Micro Labs Limited
Substance Name	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength	5; 12.5; 20
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]