Skip to main content

MedPath Trial Home

Organizations News Research

Data Sources:ClinicalTrials.govEU CTRFDAEMANMPATGAHealth CanadaWHO ICTRP

MedPath Trial Home

Search trials. Track pipelines. Understand approvals. With AI-powered intelligence for clinical research.

Product

Clinical Trials
Drug Intelligence
Global Approvals
AI Research
Pricing

Resources

FAQ
Search

Company

News
About
Contact

Legal

Privacy Policy
Terms of Service

Disclaimer: This website provides information retrieval and data analysis services. The content does not constitute medical advice. Eligibility assessments are for reference only and should not replace consultation with qualified healthcare professionals. Data is sourced from public registries and regulatory agencies; MedPath does not guarantee completeness or accuracy. Always verify information with primary sources.

© 2026 MedPath Trial. All rights reserved.

We value your privacy

We use cookies to analyze site traffic and improve your experience. See our Privacy Policy.

Fludalt Duo - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Fludalt Duo

Approved

STANDARD

Fludalt Duo

Laboratorios Liconsa, S.A.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 995a1130b2b48665
Company: Laboratorios Liconsa, S.A.
Type: Standard

Approval Details

Approval Id: 995a1130b2b48665
Drug Approval Philippines Name: Fludalt Duo
Product Name: Fludalt Duo
Registration Number: DRP-9313
Brand Name: Fludalt Duo
Generic Name: Salmeterol (as xinofoate)/Fluticasone propionate
Dosage Form: Dry Powder for Inhalation (DPI)
Dosage Strength: 100mcg/ 50mcg
Manufacturer: Laboratorios Liconsa, S.A.
Importer: Exeltis Philippine Inc.
Distributor: Exeltis Philippine Inc.
Company Detail Path: /organization/laboratorios-liconsa-sa
Issuance Date: 27 November 2020
Expiry Date: 27 November 2025
Classification: Prescription Drug (Rx)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

995a1130b2b48665

Type

Standard

Back to Philippines FDA Approvals