Glyburide - 0093-8342-01 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 0093-8342
Proprietary Name: Glyburide
Non Proprietary Name: Glyburide
Active Ingredient(s): 1.25    mg/1 & nbsp;   Glyburide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide

Product NDC: 0093-8342
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074388
Marketing Category: ANDA
Start Marketing Date: 19950830

Package Information of Glyburide

Package NDC: 0093-8342-01
Package Description: 100 TABLET in 1 BOTTLE (0093-8342-01)

NDC Information of Glyburide

NDC Code 0093-8342-01
Proprietary Name Glyburide
Package Description 100 TABLET in 1 BOTTLE (0093-8342-01)
Product NDC 0093-8342
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950830
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name GLYBURIDE
Strength Number 1.25
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information