Skip to main content

Clinical TrialsSearch 1M+ trials from global registries Drug IntelligenceFollow pipelines from discovery to approval

Global ApprovalsTrack regulatory decisions across 12+ agencies

US FDA Drugs EU EMA Drugs Singapore HSA Drugs China NMPA Drugs Australia TGA Drugs Canada HC Drugs Spain CIMA-AEMPS Drugs UK EMC Drugs Saudi SFDA Drugs Malaysia NPRA Drugs Philippines FDA Drugs Kenya PPB Drugs

AI-Powered ResearchDiscover powerful insights with advanced AI analysis tools for clinical trials.Learn more →Premium AccessGet unlimited access to our comprehensive pharmaceutical database and analytics.Subscribe →

Organizations News Research

Data Sources:ClinicalTrials.govEU CTRFDAEMANMPATGAHealth CanadaWHO ICTRP

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. All rights reserved.

We value your privacy

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

VANFLYTA TABLETS 26.5MG - PPB Drug Approval Details

Approvals/PPB/VANFLYTA TABLETS 26.5MG

Approved

STANDARD

VANFLYTA TABLETS 26.5MG

DAIICHI SANKYO HONG KONG LIMITED🇰🇪 Pharmacy and Poisons Board

Approval Date: May 30, 2025
Approval ID: 8563b523b23facc5
Company: DAIICHI SANKYO HONG KONG LIMITED
Type: Standard

Approval Details

Approval Id: 8563b523b23facc5
Product Name: VANFLYTA TABLETS 26.5MG
Drug Hk Name: VANFLYTA TABLETS 26.5MG
Registration Code: HK-68662
Company Name: DAIICHI SANKYO HONG KONG LIMITED
Company Detail Path: /organization/1469dbae1bbe0175/daiichi-sankyo-hong-kong-limited
Registration Category: Part 1, Schedule 1 & Schedule 3 Poison
Sale Requirement: Prescription only Medicines
Registration Date: 2025-04-25
Company Address: SUITES 3207-11, 32/F, TOWER ONE, TIMES SQUARE, 1, MATHESON STREET, CAUSEWAY BAY, HONG KONG

Active Ingredients

Approved

Quick Info

Agency

PPB

Country

🇰🇪

Approval Date

May 30, 2025

Approval ID

8563b523b23facc5

Type

Standard

Back to PPB Approvals