Glipizide - 0228-2899-96 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 0228-2899
Proprietary Name: Glipizide
Non Proprietary Name: Glipizide
Active Ingredient(s): 5    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 0228-2899
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076467
Marketing Category: ANDA
Start Marketing Date: 20030908

Package Information of Glipizide

Package NDC: 0228-2899-96
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-2899-96)

NDC Information of Glipizide

NDC Code 0228-2899-96
Proprietary Name Glipizide
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0228-2899-96)
Product NDC 0228-2899
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030908
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth LLC
Substance Name GLIPIZIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information