"61919-785-90" National Drug Code (NDC)

Losartan Potassium And Hydrochlorothiazide 90 TABLET in 1 BOTTLE (61919-785-90)
(DIRECT RX)

NDC Code61919-785-90
Package Description90 TABLET in 1 BOTTLE (61919-785-90)
Product NDC61919-785
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium And Hydrochlorothiazide
Non-Proprietary NameLosartan Potassium And Hydrochlorothiazide
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA090528
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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