Riluzole 68462-0381
Product NDC
68462-0381- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 18, 2013
- Listing Expires
- December 31, 2026
- Application
- ANDA091394
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Riluzole | 50 mg/1 |
Drug Class
Benzothiazole [EPC]Benzothiazole [EPC]Benzothiazoles [CS]
Packaging Options(2)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-381-10)
60 TABLET, FILM COATED in 1 BOTTLE (68462-381-60)