"0603-4228-32" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 1000 TABLET, FILM COATED in 1 BOTTLE (0603-4228-32)
(Qualitest Pharmaceuticals)

NDC Code0603-4228-32
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0603-4228-32)
Product NDC0603-4228
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20130215
End Marketing Date20170731
Marketing Category NameANDA
Application NumberANDA091617
ManufacturerQualitest Pharmaceuticals
Substance NameLOSARTAN POTASSIUM; HYDROCHLOROTHIAZIDE
Strength50; 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]

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