"0591-3750-19" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3750-19)
(Watson Laboratories, Inc.)

NDC Code0591-3750-19
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3750-19)
Product NDC0591-3750
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20110112
Marketing Category NameANDA
Application NumberANDA200180
ManufacturerWatson Laboratories, Inc.
Substance NameLOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
Strength100; 25
Strength Unitmg/1; mg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]

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