"71335-0036-5" National Drug Code (NDC)

Glipizide 20 TABLET in 1 BOTTLE (71335-0036-5)
(Bryant Ranch Prepack)

NDC Code71335-0036-5
Package Description20 TABLET in 1 BOTTLE (71335-0036-5)
Product NDC71335-0036
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20110718
Marketing Category NameANDA
Application NumberANDA074550
ManufacturerBryant Ranch Prepack
Substance NameGLIPIZIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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