CABAZITAXEL
Summary
FDA approved CABAZITAXEL by ACTAVIS. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2024-03-14. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA207970-1
Action Date
2024-03-14
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
CABAZITAXEL, SOLUTION, INTRAVENOUS. Application: NDA207970
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 "NDA207970-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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