"71335-2099-3" National Drug Code (NDC)

Irbesartan And Hydrochlorothiazide 28 TABLET in 1 BOTTLE (71335-2099-3)
(Bryant Ranch Prepack)

NDC Code71335-2099-3
Package Description28 TABLET in 1 BOTTLE (71335-2099-3)
Product NDC71335-2099
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIrbesartan And Hydrochlorothiazide
Non-Proprietary NameIrbesartan And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20140301
Marketing Category NameANDA
Application NumberANDA203072
ManufacturerBryant Ranch Prepack
Substance NameHYDROCHLOROTHIAZIDE; IRBESARTAN
Strength12.5; 150
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]

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