ELEPSIA XR 1000 MG (LEVETIRACETAM)
Summary
FDA approved ELEPSIA XR 1000 MG (LEVETIRACETAM) by TRIPOINT. NDA (New Drug) approval (Labeling) on 2024-03-12. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
NDA204417-9
Action Date
2024-03-12
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
ELEPSIA XR 1000 MG (generic: LEVETIRACETAM), TABLET, EXTENDED RELEASE, ORAL. Application: NDA204417
Company
Context & Analysis
Frequently Asked Questions
How often does TRIPOINT have FDA actions?
This is the only FDA action we have on record for TRIPOINT in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA204417-9" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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