ABIRATERONE ACETATE
Summary
FDA approved ABIRATERONE ACETATE by TEVA PHARMS USA. ANDA (Generic) approval on 2022-06-24. TABLET, ORAL.
Details
Source
Drug Approval
External ID
ANDA212206-1
Action Date
2022-06-24
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
ABIRATERONE ACETATE, TABLET, ORAL. Application: ANDA212206
Company
Context & Analysis
TEVA PHARMS USA has 39 FDA actions in our database.
Frequently Asked Questions
How often does TEVA PHARMS USA have FDA actions?
TEVA PHARMS USA has 39 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 "ANDA212206-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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