approval · primary record
VUTRISIRAN SODIUM
FDA · NDA · 2025-03-20
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2025-03-20 |
| Brand | AMVUTTRA |
| Sponsor | ALNYLAM PHARMS INC |
| Route | SUBCUTANEOUS |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T03:30:54.974Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:VUTRISIRAN SODIUM:2025-03-20
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