24987-700 : Rilutek 50 mg Oral Tablet
NDC: | 24987-700 |
Labeler: | Covis Pharmaceuticals, Inc. |
Product Type: | Human Prescription Drug |
Drug Name: | Rilutek |
Dosage Form: | Oral Tablet |
Application #: | NDA020599 |
Rev. Date: |
Appearance:
Markings: | RPR;202 |
Shapes: |
Oval |
Colors: |
White |
Size (mm): | 10 |
Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 24987-700-60: 1 BOTTLE IN 1 CARTON (24987‑700‑60) > 60 TABLET IN 1 BOTTLE
Active Ingredients:
- Riluzole
Dosage Strength:
- 50 mg
Inactive Ingredients:
- Calcium Phosphate, Dibasic, Anhydrous
- Cellulose, Microcrystalline
- Silicon Dioxide
- Magnesium Stearate
- Croscarmellose Sodium
- Hypromelloses
- Polyethylene Glycol 6000
- Titanium Dioxide
Pharmaceutical Classes:
- Benzothiazole [EPC]
- Benzothiazoles [Chemical/Ingredient]
Related Products:
Based on records with the same trade name.- 0075-7700 Rilutek 50 mg Oral Tablet by Sanofi-aventis U.S. LLC
- 0179-0143 Rilutek 50 mg/1 Oral Tablet by Kaiser Foundation Hospitals
- 70515-700 Rilutek 50 mg Oral Tablet by Covis Pharma
NDC QR Code
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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.