Glyburide - 50436-6409-2 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 50436-6409
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: 50436-6409
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074388
Marketing Category: ANDA
Start Marketing Date: 20110718

Package Information of Glyburide

Package NDC: 50436-6409-2
Package Description: 60 TABLET in 1 BOTTLE (50436-6409-2)

NDC Information of Glyburide

NDC Code 50436-6409-2
Proprietary Name Glyburide
Package Description 60 TABLET in 1 BOTTLE (50436-6409-2)
Product NDC 50436-6409
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110718
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name GLYBURIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information