BORTEZOMIB
Summary
FDA approved BORTEZOMIB by EUGIA PHARMA. ANDA (Generic) approval on 2022-05-02. INJECTABLE, INTRAVENOUS, SUBCUTANEOUS.
Details
Source
Drug Approval
External ID
ANDA212825-1
Action Date
2022-05-02
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
BORTEZOMIB, INJECTABLE, INTRAVENOUS, SUBCUTANEOUS. Application: ANDA212825
Company
Context & Analysis
EUGIA PHARMA has 44 FDA actions in our database.
Frequently Asked Questions
How often does EUGIA PHARMA have FDA actions?
EUGIA PHARMA has 44 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 "ANDA212825-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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