Glucotrol - 0049-0174-02 - (GLIPIZIDE)

Alphabetical Index


Drug Information of Glucotrol

Product NDC: 0049-0174
Proprietary Name: Glucotrol
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 Glucotrol

Product NDC: 0049-0174
Labeler Name: Roerig
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020329
Marketing Category: NDA
Start Marketing Date: 20130509

Package Information of Glucotrol

Package NDC: 0049-0174-02
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0049-0174-02)

NDC Information of Glucotrol

NDC Code 0049-0174-02
Proprietary Name Glucotrol
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0049-0174-02)
Product NDC 0049-0174
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GLIPIZIDE
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130509
Marketing Category Name NDA
Labeler Name Roerig
Substance Name GLIPIZIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glucotrol


General Information