Glyburide - 49349-730-02 - (Glyburide)

Alphabetical Index


Drug Information of Glyburide

Product NDC: 49349-730
Proprietary Name: Glyburide
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 Glyburide

Product NDC: 49349-730
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076257
Marketing Category: ANDA
Start Marketing Date: 20110823

Package Information of Glyburide

Package NDC: 49349-730-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-730-02)

NDC Information of Glyburide

NDC Code 49349-730-02
Proprietary Name Glyburide
Package Description 30 TABLET in 1 BLISTER PACK (49349-730-02)
Product NDC 49349-730
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Glyburide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110823
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name GLYBURIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of Glyburide


General Information