Dimethyl Fumarate 70710-1205
Product NDC
70710-1205- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Capsule, Delayed Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 28, 2020
- Listing Expires
- December 31, 2026
- Application
- ANDA210538
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dimethyl Fumarate | 240 mg/1 |
Packaging Options(2)
60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1205-6)
46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70710-1205-8)