"70518-3398-0" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3398-0)
(REMEDYREPACK INC.)

NDC Code70518-3398-0
Package Description90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3398-0)
Product NDC70518-3398
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20220330
Marketing Category NameANDA
Application NumberANDA204901
ManufacturerREMEDYREPACK 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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