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"33342-245-10" National Drug Code (NDC)

Olmesartan Medoxomil Amlodipine And Hydrochlorothiazide 90 TABLET, FILM COATED in 1 BOTTLE (33342-245-10)
(Macleods Pharmaceuticals Limited)

NDC Code33342-245-10
Package Description90 TABLET, FILM COATED in 1 BOTTLE (33342-245-10)
Product NDC33342-245
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil Amlodipine And Hydrochlorothiazide
Non-Proprietary NameOlmesartan Medoxomil Amlodipine And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20250718
Marketing Category NameANDA
Application NumberANDA207088
ManufacturerMacleods Pharmaceuticals Limited
Substance NameAMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength5; 25; 40
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesAngiotensin 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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/33342-245-10





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