GLIPIZIDE - 49349-092-02 - (GLIPIZIDE)

Alphabetical Index


Drug Information of GLIPIZIDE

Product NDC: 49349-092
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: 49349-092
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 20101123

Package Information of GLIPIZIDE

Package NDC: 49349-092-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-092-02)

NDC Information of GLIPIZIDE

NDC Code 49349-092-02
Proprietary Name GLIPIZIDE
Package Description 30 TABLET in 1 BLISTER PACK (49349-092-02)
Product NDC 49349-092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GLIPIZIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101123
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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