"71335-2050-4" National Drug Code (NDC)

Glipizide 90 TABLET in 1 BOTTLE (71335-2050-4)
(Bryant Ranch Prepack)

NDC Code71335-2050-4
Package Description90 TABLET in 1 BOTTLE (71335-2050-4)
Product NDC71335-2050
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20020925
Marketing Category NameANDA
Application NumberANDA075795
ManufacturerBryant Ranch Prepack
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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