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Flutiright S-500 - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Flutiright S-500
Approved
STANDARD
Flutiright S-500
Biodeal Pharmaceuticals Pvt. Ltd.
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
48235c0f756294c9
Company
Biodeal Pharmaceuticals Pvt. Ltd.
Type
Standard
Approval Details
Approval Id
48235c0f756294c9
Drug Approval Philippines Name
Flutiright S-500
Product Name
Flutiright S-500
Registration Number
DRP-10106
Brand Name
Flutiright S-500
Generic Name
Salmeterol (Xinafoate) + Fluticasone Propionate
Dosage Form
Dry Powder For Inhalation In Capsule
Dosage Strength
50 mcg/500 mcg
Manufacturer
Biodeal Pharmaceuticals Pvt. Ltd.
Importer
MedEthix, Inc.
Distributor
MedEthix, Inc.
Issuance Date
26 July 2021
Expiry Date
18 August 2026
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
48235c0f756294c9
Type
Standard
Back to Philippines FDA Approvals