Riluzole 69076-0200
Product NDC
69076-0200- Manufacturer
- Florida Pharmaceutical Products, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA206045
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Riluzole | 50 mg/1 |
Drug Class
Benzothiazole [EPC]Benzothiazole [EPC]Benzothiazoles [CS]
Packaging Options(1)
60 TABLET, FILM COATED in 1 BOTTLE (69076-200-60)