Glyburide - 23155-058-10 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 23155-058
Proprietary Name: Glyburide
Non Proprietary Name: Glyburide
Active Ingredient(s): 5    mg/1 & nbsp;   Glyburide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide

Product NDC: 23155-058
Labeler Name: Heritage Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090937
Marketing Category: ANDA
Start Marketing Date: 20101005

Package Information of Glyburide

Package NDC: 23155-058-10
Package Description: 1000 TABLET in 1 BOTTLE (23155-058-10)

NDC Information of Glyburide

NDC Code 23155-058-10
Proprietary Name Glyburide
Package Description 1000 TABLET in 1 BOTTLE (23155-058-10)
Product NDC 23155-058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101005
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc.
Substance Name GLYBURIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information