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"61919-287-90" National Drug Code (NDC)

Glipizide 90 TABLET in 1 BOTTLE (61919-287-90)
(DIRECT RX)

NDC Code61919-287-90
Package Description90 TABLET in 1 BOTTLE (61919-287-90)
Product NDC61919-287
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20170220
Marketing Category NameANDA
Application NumberANDA075795
ManufacturerDIRECT RX
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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