"0093-5002-98" National Drug Code (NDC)

Olmesartan Medoxomil, Amlodipine And Hydrochlorothiazide 90 TABLET, FILM COATED in 1 BOTTLE (0093-5002-98)
(Teva Pharmaceuticals USA, Inc.)

NDC Code0093-5002-98
Package Description90 TABLET, FILM COATED in 1 BOTTLE (0093-5002-98)
Product NDC0093-5002
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 NameOLMESARTAN MEDOXOMIL; AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE
Strength40; 10; 25
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]

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