approval · primary record
LURASIDONE HYDROCHLORIDE
FDA · NDA · 2025-01-22
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2025-01-22 |
| Brand | LATUDA |
| Sponsor | SUNOVION PHARMS INC |
| Route | ORAL |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:35:16.756Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:LURASIDONE HYDROCHLORIDE:2025-01-22
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