approval · primary record
LUMASIRAN SODIUM
FDA · NDA · 2025-04-04
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2025-04-04 |
| Brand | OXLUMO |
| Sponsor | ALNYLAM PHARMS INC |
| Route | SUBCUTANEOUS |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:35:42.663Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:LUMASIRAN SODIUM:2025-04-04
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