FDA NDC Directory · JSON-LD · Markdown
NDC 43547-025 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE
| Generic name | dimethyl fumarate |
|---|---|
| Labeler / Manufacturer | Solco Healthcare US, LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA210414 |
| Dosage form / route | CAPSULE, DELAYED RELEASE · ORAL |
| Active ingredients | DIMETHYL FUMARATE (240 mg/1) |
| Marketing started | 20221018 |
| Package count | 2 |
Source: openFDA. Public-domain (CC0).