WOMENS ROGAINE UNSCENTED (MINOXIDIL)
Summary
FDA approved WOMENS ROGAINE UNSCENTED (MINOXIDIL) by KENVUE BRANDS. NDA (New Drug) approval (Labeling) on 2026-01-14. SOLUTION, TOPICAL.
Details
Source
Drug Approval
External ID
NDA019501-36
Action Date
2026-01-14
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
WOMENS ROGAINE UNSCENTED (generic: MINOXIDIL), SOLUTION, TOPICAL. Application: NDA019501
Company
Context & Analysis
KENVUE BRANDS has 3 FDA actions in our database.
Frequently Asked Questions
How often does KENVUE BRANDS have FDA actions?
KENVUE BRANDS has 3 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 "NDA019501-36" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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