Glyburide - 54868-4842-0 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 54868-4842
Proprietary Name: Glyburide
Non Proprietary Name: Glyburide
Active Ingredient(s): 6    mg/1 & nbsp;   Glyburide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Glyburide

Product NDC: 54868-4842
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074686
Marketing Category: ANDA
Start Marketing Date: 20030702

Package Information of Glyburide

Package NDC: 54868-4842-0
Package Description: 100 TABLET in 1 BOTTLE (54868-4842-0)

NDC Information of Glyburide

NDC Code 54868-4842-0
Proprietary Name Glyburide
Package Description 100 TABLET in 1 BOTTLE (54868-4842-0)
Product NDC 54868-4842
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030702
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name GLYBURIDE
Strength Number 6
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information