Home > National Drug Code (NDC) > GLIMEPIRIDE

GLIMEPIRIDE - 54458-966-10 - (GLIMEPIRIDE)

Alphabetical Index


Drug Information of GLIMEPIRIDE

Product NDC: 54458-966
Proprietary Name: GLIMEPIRIDE
Non Proprietary Name: GLIMEPIRIDE
Active Ingredient(s): 4    mg/1 & nbsp;   GLIMEPIRIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of GLIMEPIRIDE

Product NDC: 54458-966
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077091
Marketing Category: ANDA
Start Marketing Date: 20090206

Package Information of GLIMEPIRIDE

Package NDC: 54458-966-10
Package Description: 30 TABLET in 1 BLISTER PACK (54458-966-10)

NDC Information of GLIMEPIRIDE

NDC Code 54458-966-10
Proprietary Name GLIMEPIRIDE
Package Description 30 TABLET in 1 BLISTER PACK (54458-966-10)
Product NDC 54458-966
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name GLIMEPIRIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090206
Marketing Category Name ANDA
Labeler Name International Labs, Inc.
Substance Name GLIMEPIRIDE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Sulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Complete Information of GLIMEPIRIDE


General Information