BUSULFAN
Summary
FDA approved BUSULFAN by ACTAVIS. ANDA (Generic) approval (Labeling) on 2026-03-18. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
ANDA205139-5
Action Date
2026-03-18
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BUSULFAN, INJECTABLE, INJECTION. Application: ANDA205139
Company
Context & Analysis
ACTAVIS has 2 FDA actions in our database.
Frequently Asked Questions
How often does ACTAVIS have FDA actions?
ACTAVIS 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 "ANDA205139-5" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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