Glyburide - 64720-125-11 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 64720-125
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: 64720-125
Labeler Name: CorePharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076257
Marketing Category: ANDA
Start Marketing Date: 20020806

Package Information of Glyburide

Package NDC: 64720-125-11
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (64720-125-11)

NDC Information of Glyburide

NDC Code 64720-125-11
Proprietary Name Glyburide
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (64720-125-11)
Product NDC 64720-125
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020806
Marketing Category Name ANDA
Labeler Name CorePharma, LLC
Substance Name GLYBURIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information