BORTEZOMIB
Summary
FDA approved BORTEZOMIB by MAIA PHARMS INC. NDA (New Drug) approval (Type 5 - New Formulation or New Manufacturer) on 2022-07-27. SOLUTION, INTRAVENOUS.
Details
Source
Drug Approval
External ID
NDA215331-1
Action Date
2022-07-27
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
BORTEZOMIB, SOLUTION, INTRAVENOUS. Application: NDA215331
Company
Context & Analysis
Frequently Asked Questions
How often does MAIA PHARMS INC have FDA actions?
This is the only FDA action we have on record for MAIA PHARMS INC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA215331-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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