Glipizide - 53808-0259-1 - (Glipizide)

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Drug Information of Glipizide

Product NDC: 53808-0259
Proprietary Name: Glipizide
Non Proprietary Name: Glipizide
Active Ingredient(s): 10    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 53808-0259
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074305
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Glipizide

Package NDC: 53808-0259-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0259-1)

NDC Information of Glipizide

NDC Code 53808-0259-1
Proprietary Name Glipizide
Package Description 30 TABLET in 1 BLISTER PACK (53808-0259-1)
Product NDC 53808-0259
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information