LENALIDOMIDE
Summary
FDA approved LENALIDOMIDE by BIOCON PHARMA. ANDA (Generic) approval (REMS) on 2026-04-27. CAPSULE, ORAL.
Details
Source
Drug Approval
External ID
ANDA215759-2
Action Date
2026-04-27
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LENALIDOMIDE, CAPSULE, ORAL. Application: ANDA215759
Company
Context & Analysis
BIOCON PHARMA has 10 FDA actions in our database.
Frequently Asked Questions
How often does BIOCON PHARMA have FDA actions?
BIOCON PHARMA has 10 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 "ANDA215759-2" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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