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Rilutek
Rilutek - 0075-7700-60 - (riluzole)
Drug Information of Rilutek
| Product NDC: | 0075-7700 |
| Proprietary Name: | Rilutek |
| Non Proprietary Name: | riluzole |
| Active Ingredient(s): | 50 mg/1 & nbsp; riluzole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rilutek
| Product NDC: | 0075-7700 |
| Labeler Name: | sanofi-aventis U.S. LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020599 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19951212 |
Package Information of Rilutek
| Package NDC: | 0075-7700-60 |
| Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (0075-7700-60) |
NDC Information of Rilutek
| NDC Code | 0075-7700-60 |
| Proprietary Name | Rilutek |
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (0075-7700-60) |
| Product NDC | 0075-7700 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | riluzole |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19951212 |
| Marketing Category Name | NDA |
| Labeler Name | sanofi-aventis U.S. LLC |
| Substance Name | RILUZOLE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzothiazole [EPC],Benzothiazoles [Chemical/Ingredient] |
