"68071-1952-3" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 30 TABLET, FILM COATED in 1 BOTTLE (68071-1952-3)
(NuCare Pharmaceuticals, Inc.)

NDC Code68071-1952-3
Package Description30 TABLET, FILM COATED in 1 BOTTLE (68071-1952-3)
Product NDC68071-1952
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
ManufacturerNuCare Pharmaceuticals, 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 [CS]

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