ICOSAPENT ETHYL
Summary
FDA approved ICOSAPENT ETHYL by XIAMEN LP PHARM CO. ANDA (Generic) approval on 2025-08-06. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA219156-1
Action Date
2025-08-06
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ICOSAPENT ETHYL, CAPSULE, ORAL. Application: ANDA219156
Company
Context & Analysis
XIAMEN LP PHARM CO has 5 FDA actions in our database.
Frequently Asked Questions
How often does XIAMEN LP PHARM CO have FDA actions?
XIAMEN LP PHARM CO has 5 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 "ANDA219156-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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