NDC 59651-084
Dimethyl Fumarate 240 mg capsule, delayed release
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Tirupati, India | Makes it and tests it | Problems found, fixed voluntarilyDec 17, 2025 · 5 inspections |
Product details
- Generic drug
- Monomethyl: every company that makes it
- Form
- capsule, delayed release, oral
- Strength
- 240 mg
- Approval
- ANDA ANDA210385
- On the market since
- Dec 22, 2022
- Package NDCs
59651-084-60- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2024
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