LEXETTE (HALOBETASOL PROPIONATE)
Summary
FDA approved LEXETTE (HALOBETASOL PROPIONATE) by PADAGIS ISRAEL. ANDA (Generic) approval on 2023-08-11. AEROSOL, FOAM, TOPICAL.
Details
Source
Drug Approval
External ID
ANDA215266-1
Action Date
2023-08-11
Status
Approved
Category
drug
Product Code
ANDA (Generic)
Product Description
LEXETTE (generic: HALOBETASOL PROPIONATE), AEROSOL, FOAM, TOPICAL. Application: ANDA215266
Company
Context & Analysis
PADAGIS ISRAEL has 11 FDA actions in our database.
Frequently Asked Questions
How often does PADAGIS ISRAEL have FDA actions?
PADAGIS ISRAEL has 11 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 "ANDA215266-1" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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