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Seretide 250 Diskus - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Seretide 250 Diskus

Approved

STANDARD

Seretide 250 Diskus

Glaxo Wellcome Production.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: ef73ad2f3015a46b
Company: Glaxo Wellcome Production.
Type: Standard

Approval Details

Approval Id: ef73ad2f3015a46b
Drug Approval Philippines Name: Seretide 250 Diskus
Product Name: Seretide 250 Diskus
Registration Number: DR-XY25841
Brand Name: Seretide 250 Diskus
Generic Name: Salmeterol (As Xinafoate) + Fluticasone Propionate
Dosage Form: Dry Powder For Inhalation
Dosage Strength: 50 mcg/ 250 mcg per dose
Manufacturer: Glaxo Wellcome Production.
Importer: GlaxoSmithKline Philippines, Inc.
Distributor: GlaxoSmithKline Philippines, Inc.
Issuance Date: 31 July 2023
Expiry Date: 31 July 2028
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

ef73ad2f3015a46b

Type

Standard

Back to Philippines FDA Approvals