Glipizide - 60429-082-01 - (Glipizide)

Alphabetical Index


Drug Information of Glipizide

Product NDC: 60429-082
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: 60429-082
Labeler Name: Golden State Medical Supply Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075795
Marketing Category: ANDA
Start Marketing Date: 20120920

Package Information of Glipizide

Package NDC: 60429-082-01
Package Description: 100 TABLET in 1 BOTTLE (60429-082-01)

NDC Information of Glipizide

NDC Code 60429-082-01
Proprietary Name Glipizide
Package Description 100 TABLET in 1 BOTTLE (60429-082-01)
Product NDC 60429-082
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glipizide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120920
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply 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