approval · primary record
DONIDALORSEN SODIUM
FDA · NDA · 2025-08-21
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2025-08-21 |
| Brand | DAWNZERA (AUTOINJECTOR) |
| Sponsor | IONIS PHARMS INC |
| Route | SUBCUTANEOUS |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:35:23.316Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:DONIDALORSEN SODIUM:2025-08-21
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