"52125-479-23" National Drug Code (NDC)

Glipizide 180 TABLET in 1 BOTTLE (52125-479-23)
(REMEDYREPACK INC.)

NDC Code52125-479-23
Package Description180 TABLET in 1 BOTTLE (52125-479-23)
Product NDC52125-479
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20150317
End Marketing Date20170815
Marketing Category NameANDA
Application NumberANDA074550
ManufacturerREMEDYREPACK INC.
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

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