DiaBeta - 0039-0051-10 - (glyburide)

Alphabetical Index


Drug Information of DiaBeta

Product NDC: 0039-0051
Proprietary Name: DiaBeta
Non Proprietary Name: glyburide
Active Ingredient(s): 2.5    mg/1 & nbsp;   glyburide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DiaBeta

Product NDC: 0039-0051
Labeler Name: Sanofi-Aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017532
Marketing Category: NDA
Start Marketing Date: 20090601

Package Information of DiaBeta

Package NDC: 0039-0051-10
Package Description: 100 TABLET in 1 BOTTLE (0039-0051-10)

NDC Information of DiaBeta

NDC Code 0039-0051-10
Proprietary Name DiaBeta
Package Description 100 TABLET in 1 BOTTLE (0039-0051-10)
Product NDC 0039-0051
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name NDA
Labeler Name Sanofi-Aventis U.S. LLC
Substance Name GLYBURIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of DiaBeta


General Information