GlyBURIDE - 67253-462-10 - (GlyBURIDE)

Alphabetical Index


Drug Information of GlyBURIDE

Product NDC: 67253-462
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: 67253-462
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074591
Marketing Category: ANDA
Start Marketing Date: 19971222

Package Information of GlyBURIDE

Package NDC: 67253-462-10
Package Description: 100 TABLET in 1 BOTTLE (67253-462-10)

NDC Information of GlyBURIDE

NDC Code 67253-462-10
Proprietary Name GlyBURIDE
Package Description 100 TABLET in 1 BOTTLE (67253-462-10)
Product NDC 67253-462
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GlyBURIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19971222
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, 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