"61919-713-30" National Drug Code (NDC)

Glipizide 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-713-30)
(Direct_Rx)

NDC Code61919-713-30
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (61919-713-30)
Product NDC61919-713
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190321
Marketing Category NameANDA
Application NumberANDA204720
ManufacturerDirect_Rx
Substance NameGLIPIZIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]

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