CRENESSITY (CRINECERFONT)
Summary
FDA approved CRENESSITY (CRINECERFONT) by NEUROCRINE. NDA (New Drug) approval (Type 1 - New Molecular Entity) on 2024-12-13. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
NDA218808-1
Action Date
2024-12-13
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
CRENESSITY (generic: CRINECERFONT), CAPSULE, ORAL. Application: NDA218808
Company
Context & Analysis
NEUROCRINE has 2 FDA actions in our database.
Frequently Asked Questions
How often does NEUROCRINE have FDA actions?
NEUROCRINE has 2 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 "NDA218808-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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