OXYTROL (OXYBUTYNIN)
Summary
FDA approved OXYTROL (OXYBUTYNIN) by ALLERGAN. NDA (New Drug) approval (Labeling) on 2024-05-29. FILM, EXTENDED RELEASE, TRANSDERMAL.
Details
Source
Drug Approval
External ID
NDA021351-20
Action Date
2024-05-29
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
OXYTROL (generic: OXYBUTYNIN), FILM, EXTENDED RELEASE, TRANSDERMAL. Application: NDA021351
Company
Context & Analysis
ALLERGAN has 5 FDA actions in our database.
Frequently Asked Questions
How often does ALLERGAN have FDA actions?
ALLERGAN has 5 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 "NDA021351-20" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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