Ketek - 0088-2225-49 - (telithromycin)

Alphabetical Index


Drug Information of Ketek

Product NDC: 0088-2225
Proprietary Name: Ketek
Non Proprietary Name: telithromycin
Active Ingredient(s): 400    mg/1 & nbsp;   telithromycin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ketek

Product NDC: 0088-2225
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021144
Marketing Category: NDA
Start Marketing Date: 20100601

Package Information of Ketek

Package NDC: 0088-2225-49
Package Description: 10 BLISTER PACK in 1 BOX (0088-2225-49) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ketek

NDC Code 0088-2225-49
Proprietary Name Ketek
Package Description 10 BLISTER PACK in 1 BOX (0088-2225-49) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 0088-2225
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name telithromycin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100601
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name TELITHROMYCIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Ketolide Antibacterial [EPC],Ketolides [Chemical/Ingredient]

Complete Information of Ketek


General Information