"68180-212-03" National Drug Code (NDC)

Losartan Potassium 1000 TABLET in 1 BOTTLE (68180-212-03)
(Lupin Pharmaceuticals, Inc.)

NDC Code68180-212-03
Package Description1000 TABLET in 1 BOTTLE (68180-212-03)
Product NDC68180-212
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET
UsageORAL
Start Marketing Date20101006
End Marketing Date20181231
Marketing Category NameANDA
Application NumberANDA078232
ManufacturerLupin Pharmaceuticals, Inc.
Substance NameLOSARTAN POTASSIUM
Strength100
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

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