LEVETIRACETAM
Summary
FDA approved LEVETIRACETAM by ACTAVIS MID ATLANTIC. ANDA (Generic) approval (Labeling) on 2025-03-04. SOLUTION, ORAL.
Details
Source
Drug Approval
External ID
ANDA078976-22
Action Date
2025-03-04
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LEVETIRACETAM, SOLUTION, ORAL. Application: ANDA078976
Company
Context & Analysis
ACTAVIS MID ATLANTIC has 6 FDA actions in our database.
Frequently Asked Questions
How often does ACTAVIS MID ATLANTIC have FDA actions?
ACTAVIS MID ATLANTIC has 6 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 "ANDA078976-22" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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