Dimethyl Fumarate 70512-0853
Product NDC
70512-0853- Manufacturer
- Sola Pharmaceuticals, Llc
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 31, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA210436
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dimethyl Fumarate | 240 mg/1 |
Packaging Options(1)
1 BOTTLE in 1 CARTON (70512-853-60) / 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE