"71335-0152-4" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)
(Bryant Ranch Prepack)

NDC Code71335-0152-4
Package Description120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)
Product NDC71335-0152
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20101006
Marketing Category NameANDA
Application NumberANDA091629
ManufacturerBryant Ranch Prepack
Substance NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength12.5; 50
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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