RELEUKO (FILGRASTIM)
Summary
FDA approved RELEUKO (FILGRASTIM) by KASHIV BIOSCIENCES LLC. BLA (Biologic) approval on 2025-04-29. SOLUTION, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
BLA761082-14
Action Date
2025-04-29
Status
Approved
Category
drug
Product Code
BLA (Biologic)
Product Description
RELEUKO (generic: FILGRASTIM), SOLUTION, SUBCUTANEOUS. Application: BLA761082
Company
Context & Analysis
KASHIV BIOSCIENCES LLC has 2 FDA actions in our database.
Frequently Asked Questions
How often does KASHIV BIOSCIENCES LLC have FDA actions?
KASHIV BIOSCIENCES LLC has 2 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 "BLA761082-14" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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