"0591-3749-10" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3749-10)
(Watson Laboratories, Inc.)

NDC Code0591-3749-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3749-10)
Product NDC0591-3749
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; 12.5
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0591-3749-10