approval · primary record
ASCIMINIB HYDROCHLORIDE
FDA · NDA · 2026-09-22
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2026-09-22 |
| Brand | SCEMBLIX |
| Sponsor | NOVARTIS |
| Route | ORAL |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T03:30:40.170Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:ASCIMINIB HYDROCHLORIDE:2026-09-22
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