Glyburide - 63739-119-10 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 63739-119
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: 63739-119
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074388
Marketing Category: ANDA
Start Marketing Date: 20070828

Package Information of Glyburide

Package NDC: 63739-119-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-119-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Glyburide

NDC Code 63739-119-10
Proprietary Name Glyburide
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-119-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070828
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name GLYBURIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information