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Ketek
Ketek - 0088-2225-49 - (telithromycin)
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] |
