"72189-167-90" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 90 TABLET in 1 BOTTLE (72189-167-90)
(Direct_Rx)

NDC Code72189-167-90
Package Description90 TABLET in 1 BOTTLE (72189-167-90)
Product NDC72189-167
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20210108
Marketing Category NameANDA
Application NumberANDA078245
ManufacturerDirect_Rx
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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