Rufinamide 59651-0617
Product NDC
59651-0617- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 16, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA217230
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Rufinamide | 400 mg/1 |
Packaging Options(1)
120 TABLET, FILM COATED in 1 BOTTLE (59651-617-08)