Glipizide - 0172-3649-10 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 0172-3649
Proprietary Name: Glipizide
Non Proprietary Name: Glipizide
Active Ingredient(s): 5    mg/1 & nbsp;   Glipizide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glipizide

Product NDC: 0172-3649
Labeler Name: IVAX Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074497
Marketing Category: ANDA
Start Marketing Date: 19950912

Package Information of Glipizide

Package NDC: 0172-3649-10
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-3649-10) > 1 TABLET in 1 BLISTER PACK (0172-3649-00)

NDC Information of Glipizide

NDC Code 0172-3649-10
Proprietary Name Glipizide
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-3649-10) > 1 TABLET in 1 BLISTER PACK (0172-3649-00)
Product NDC 0172-3649
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950912
Marketing Category Name ANDA
Labeler Name IVAX Pharmaceuticals Inc.
Substance Name GLIPIZIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information