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.

Approvals/Philippines FDA/Diovan

Approved

STANDARD

Diovan

Novartis Farmaceutica SA🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 501055aa81dea378
Company: Novartis Farmaceutica SA
Type: Standard

Approval Details

Approval Id: 501055aa81dea378
Drug Approval Philippines Name: Diovan
Product Name: Diovan
Registration Number: DRP-5124
Brand Name: Diovan
Generic Name: Valsartan
Dosage Form: Film-Coated Tablet
Dosage Strength: 80mg
Manufacturer: Novartis Farmaceutica SA
Importer: Novartis Healthcare Philippines, Inc.
Issuance Date: 25 August 2024
Expiry Date: 24 September 2029
Pharmacologic Category: Angiotensin II Receptor Antagonist
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

501055aa81dea378

Type

Standard

Back to Philippines FDA Approvals

Diovan - Philippines FDA Drug Approval Details