"71335-1392-1" National Drug Code (NDC)

Irbesartan And Hydrochlorothiazide 30 TABLET, FILM COATED in 1 BOTTLE (71335-1392-1)
(Bryant Ranch Prepack)

NDC Code71335-1392-1
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71335-1392-1)
Product NDC71335-1392
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameIrbesartan And Hydrochlorothiazide
Non-Proprietary NameIrbesartan And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20190930
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA020758
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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