FESOTERODINE FUMARATE
Summary
FDA approved FESOTERODINE FUMARATE by ACTAVIS LABS FL INC. ANDA (Generic) approval on 2023-01-04. TABLET, EXTENDED RELEASE, ORAL.
Details
Source
Drug Approval
External ID
ANDA204868-1
Action Date
2023-01-04
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
FESOTERODINE FUMARATE, TABLET, EXTENDED RELEASE, ORAL. Application: ANDA204868
Company
Context & Analysis
ACTAVIS LABS FL INC has 17 FDA actions in our database.
Frequently Asked Questions
How often does ACTAVIS LABS FL INC have FDA actions?
ACTAVIS LABS FL INC has 17 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 "ANDA204868-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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