Glipizide - 68788-0141-1 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 68788-0141
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: 68788-0141
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075795
Marketing Category: ANDA
Start Marketing Date: 20130218

Package Information of Glipizide

Package NDC: 68788-0141-1
Package Description: 100 TABLET in 1 BOTTLE (68788-0141-1)

NDC Information of Glipizide

NDC Code 68788-0141-1
Proprietary Name Glipizide
Package Description 100 TABLET in 1 BOTTLE (68788-0141-1)
Product NDC 68788-0141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130218
Marketing Category Name ANDA
Labeler Name Preferred 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