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XAMIOL - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
XAMIOL
Approved
STANDARD
XAMIOL
Leo Laboratories Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
9cbd4f0df1d714ef
Company
Leo Laboratories Ltd.
Type
Standard
Approval Details
Approval Id
9cbd4f0df1d714ef
Drug Approval Philippines Name
XAMIOL
Product Name
XAMIOL
Registration Number
DR-XY37761
Brand Name
XAMIOL
Generic Name
Calcipotriol (as Monohydrate) + Betamethasone (as dipropionate)
Dosage Form
Topical Gel
Dosage Strength
50 mcg/500 mcg per gram
Manufacturer
Leo Laboratories Ltd.
Importer
Zuellig Pharma Corporation
Distributor
Zuellig Pharma Corporation
Company Detail Path
/organization/leo-laboratories-ltd
Issuance Date
21 October 2024
Expiry Date
21 January 2030
Pharmacologic Category
Anti-psoriasis
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
9cbd4f0df1d714ef
Type
Standard
Back to Philippines FDA Approvals