"71205-041-90" National Drug Code (NDC)

Glipizide 90 TABLET in 1 BOTTLE (71205-041-90)
(Proficient Rx LP)

NDC Code71205-041-90
Package Description90 TABLET in 1 BOTTLE (71205-041-90)
Product NDC71205-041
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20020925
Marketing Category NameANDA
Application NumberANDA075795
ManufacturerProficient Rx LP
Substance NameGLIPIZIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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