"16571-502-50" National Drug Code (NDC)

Losartan Potassium 500 TABLET, FILM COATED in 1 BOTTLE (16571-502-50)
(Rising Pharmaceuticals, Inc)

NDC Code16571-502-50
Package Description500 TABLET, FILM COATED in 1 BOTTLE (16571-502-50)
Product NDC16571-502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLosartan Potassium
Non-Proprietary NameLosartan Potassium
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20140730
Marketing Category NameANDA
Application NumberANDA091497
ManufacturerRising Pharmaceuticals, Inc
Substance NameLOSARTAN POTASSIUM
Strength100
Strength Unitmg/1
Pharmacy ClassesAngiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

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