Rufinamide 68462-0713
Product NDC
68462-0713- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 16, 2016
- Listing Expires
- December 31, 2027
- Application
- ANDA205075
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Rufinamide | 200 mg/1 |
Packaging Options(3)
500 TABLET, FILM COATED in 1 BOTTLE (68462-713-05)
120 TABLET, FILM COATED in 1 BOTTLE (68462-713-08)
30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)