LOTRIMIN ULTRA ATHLETES FOOT (BUTENAFINE HYDROCHLORIDE)
Summary
FDA approved LOTRIMIN ULTRA ATHLETES FOOT (BUTENAFINE HYDROCHLORIDE) by BAYER HEALTHCARE LLC. NDA (New Drug) approval (Labeling) on 2024-07-10. CREAM, TOPICAL.
Details
Source
Drug Approval
External ID
NDA021307-24
Action Date
2024-07-10
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
LOTRIMIN ULTRA ATHLETES FOOT (generic: BUTENAFINE HYDROCHLORIDE), CREAM, TOPICAL. Application: NDA021307
Company
Context & Analysis
BAYER HEALTHCARE LLC has 4 FDA actions in our database.
Frequently Asked Questions
How often does BAYER HEALTHCARE LLC have FDA actions?
BAYER HEALTHCARE LLC has 4 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 "NDA021307-24" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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