LEVETIRACETAM IN SODIUM CHLORIDE (LEVETIRACETAM)
Summary
FDA approved LEVETIRACETAM IN SODIUM CHLORIDE (LEVETIRACETAM) by NEXUS. ANDA (Generic) approval (Labeling) on 2023-03-03. INJECTABLE, INTRAVENOUS.
Details
Source
Drug Approval
External ID
ANDA213532-2
Action Date
2023-03-03
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LEVETIRACETAM IN SODIUM CHLORIDE (generic: LEVETIRACETAM), INJECTABLE, INTRAVENOUS. Application: ANDA213532
Company
Context & Analysis
NEXUS has 8 FDA actions in our database.
Frequently Asked Questions
How often does NEXUS have FDA actions?
NEXUS has 8 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 "ANDA213532-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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