"70518-0112-0" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 90 TABLET in 1 BOTTLE (70518-0112-0)
(REMEDYREPACK INC.)

NDC Code70518-0112-0
Package Description90 TABLET in 1 BOTTLE (70518-0112-0)
Product NDC70518-0112
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20170110
Marketing Category NameANDA
Application NumberANDA090528
ManufacturerREMEDYREPACK INC.
Substance NameHYDROCHLOROTHIAZIDE; LOSARTAN POTASSIUM
Strength12.5; 50
Strength Unitmg/1; mg/1
Pharmacy ClassesIncreased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

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