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Gemfon - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Gemfon
Approved
STANDARD
Gemfon
PT. Fonko International Pharmaceuticals
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
21a3d930e3efb957
Company
PT. Fonko International Pharmaceuticals
Type
Standard
Approval Details
Approval Id
21a3d930e3efb957
Drug Approval Philippines Name
Gemfon
Product Name
Gemfon
Registration Number
DRP-9338
Brand Name
Gemfon
Generic Name
Gemcitabine (as hydrochloride)
Dosage Form
Lyophilized Powder For Injecttion (Iv)
Dosage Strength
1g
Manufacturer
PT. Fonko International Pharmaceuticals
Importer
Glorious Dexa Mandaya, Inc
Distributor
Glorious Dexa Mandaya, Inc
Issuance Date
26 July 2024
Expiry Date
16 January 2030
Pharmacologic Category
Antineoplastic
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
21a3d930e3efb957
Type
Standard
Back to Philippines FDA Approvals