LENALIDOMIDE
Summary
FDA approved LENALIDOMIDE by CIPLA. ANDA (Generic) approval (REMS) on 2026-04-27. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA213165-2
Action Date
2026-04-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LENALIDOMIDE, CAPSULE, ORAL. Application: ANDA213165
Company
Context & Analysis
CIPLA has 40 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
How often does CIPLA have FDA actions?
CIPLA has 40 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "ANDA213165-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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