"0093-5003-56" National Drug Code (NDC)

Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide 30 TABLET, FILM COATED in 1 BOTTLE (0093-5003-56)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5003-56
Package Description30 TABLET, FILM COATED in 1 BOTTLE (0093-5003-56)
Product NDC0093-5003
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 Date20161114
Marketing Category NameANDA
Application NumberANDA202491
ManufacturerTeva Pharmaceuticals USA, Inc.
Substance NameAMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL
Strength10; 12.5; 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]

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