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Glipizide - glipizide

Navigation: NDC > Supplier starting with: G > GREENSTONE LLC
Field Value
NDC Code: 59762-5032
Proprietary Name: Glipizide
Suffix: XL
Non-Proprietary Name: glipizide
Dosage Form: TABLET, EXTENDED RELEASE
Method: ORAL
Original Marketing Date: 11-06-2004
End of Marketing: 31-03-2017
Category Name: NDA AUTHORIZED GENERIC
Application Number: NDA020329
Labeler: GREENSTONE LLC
Substance Name: GLIPIZIDE
Active Numerator Strength: 5
Active Ingredient Unit: mg/1
Pharm Classes: Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]
DEA Schedule: