DAYBUE STIX (TROFINETIDE)
Summary
FDA approved DAYBUE STIX (TROFINETIDE) by ACADIA PHARMS INC. NDA (New Drug) approval (Type 3 - New Dosage Form) on 2025-12-11. FOR SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
NDA219884-1
Action Date
2025-12-11
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
DAYBUE STIX (generic: TROFINETIDE), FOR SOLUTION, ORAL. Application: NDA219884
Company
Context & Analysis
ACADIA PHARMS INC has 3 FDA actions in our database.
Frequently Asked Questions
How often does ACADIA PHARMS INC have FDA actions?
ACADIA PHARMS INC has 3 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA219884-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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