Glyburide - 65862-030-00 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 65862-030
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: 65862-030
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077537
Marketing Category: ANDA
Start Marketing Date: 20071018

Package Information of Glyburide

Package NDC: 65862-030-00
Package Description: 100 TABLET in 1 BOTTLE (65862-030-00)

NDC Information of Glyburide

NDC Code 65862-030-00
Proprietary Name Glyburide
Package Description 100 TABLET in 1 BOTTLE (65862-030-00)
Product NDC 65862-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20071018
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name GLYBURIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information