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"42571-249-10" National Drug Code (NDC)

Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide 1000 TABLET, FILM COATED in 1 BOTTLE (42571-249-10)
(Micro Labs Limited)

NDC Code42571-249-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (42571-249-10)
Product NDC42571-249
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameOlmesartan Medoxomil, Amlodipine And Hydrochlorothiazide
Non-Proprietary NameOlmesartan Medoxomil, Amlodipine Besylate And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20260301
Marketing Category NameANDA
Application NumberANDA207437
ManufacturerMicro Labs Limited
Substance NameAMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength10; 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/42571-249-10





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