"52125-972-20" National Drug Code (NDC)

Glipizide 100 TABLET in 1 BOTTLE (52125-972-20)
(REMEDYREPACK INC.)

NDC Code52125-972-20
Package Description100 TABLET in 1 BOTTLE (52125-972-20)
Product NDC52125-972
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20141126
Marketing Category NameANDA
Application NumberANDA077820
ManufacturerREMEDYREPACK INC.
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

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