Glipizide - 10544-192-30 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 10544-192
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: 10544-192
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074223
Marketing Category: ANDA
Start Marketing Date: 20100909

Package Information of Glipizide

Package NDC: 10544-192-30
Package Description: 30 TABLET in 1 BOTTLE (10544-192-30)

NDC Information of Glipizide

NDC Code 10544-192-30
Proprietary Name Glipizide
Package Description 30 TABLET in 1 BOTTLE (10544-192-30)
Product NDC 10544-192
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100909
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name GLIPIZIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glipizide


General Information