"0603-4230-32" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 1000 TABLET, FILM COATED in 1 BOTTLE (0603-4230-32)
(Qualitest Pharmaceuticals)

NDC Code0603-4230-32
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (0603-4230-32)
Product NDC0603-4230
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 Date20170831
Marketing Category NameANDA
Application NumberANDA091617
ManufacturerQualitest Pharmaceuticals
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0603-4230-32