"70934-862-90" National Drug Code (NDC)

Glipizide 90 TABLET in 1 BOTTLE, PLASTIC (70934-862-90)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-862-90
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70934-862-90)
Product NDC70934-862
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20210607
End Marketing Date20241031
Marketing Category NameANDA
Application NumberANDA075795
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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