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"61919-287-82" National Drug Code (NDC)

Glipizide 180 TABLET in 1 BOTTLE (61919-287-82)
(Direct_Rx)

NDC Code61919-287-82
Package Description180 TABLET in 1 BOTTLE (61919-287-82)
Product NDC61919-287
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20190820
Marketing Category NameANDA
Application NumberANDA075795
ManufacturerDirect_Rx
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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