"33342-247-07" National Drug Code (NDC)

NDC Code	33342-247-07
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (33342-247-07)
Product NDC	33342-247
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olmesartan Medoxomil Amlodipine And Hydrochlorothiazide
Non-Proprietary Name	Olmesartan Medoxomil Amlodipine And Hydrochlorothiazide
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20250718
Marketing Category Name	ANDA
Application Number	ANDA207088
Manufacturer	Macleods Pharmaceuticals Limited
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]