"68071-1613-9" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 90 TABLET, FILM COATED in 1 BOTTLE (68071-1613-9)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-1613-9
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68071-1613-9)
Product NDC68071-1613
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 NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength12.5; 100
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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