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.

VEOZAH - Health Canada Drug Approval Details

Approvals/Health Canada/VEOZAH

Authorized

STANDARD

VEOZAH

astellas pharma canada inc🇨🇦 Health Canada

Approval Date: Jul 4, 2025
Approval ID: 1fa88d0fb5be6931
Company: astellas pharma canada inc
Type: Standard

Approval Details

Approval Id: 1fa88d0fb5be6931
Drug Approval Canada Name: VEOZAH
Product Name: VEOZAH
Status: Marketed
Status Date: 2025-03-11
Original Market Date: 2025-03-11
Din: 02553600
Drug Class: Human
Dosage Form: Tablet
Route Of Administration: Oral
Schedule: Prescription
Ahfs: 28:92.00
Atc Original: G02CX06 FEZOLINETANT
Atc Name: g 02 cx 06
Aig Number: 0166344001
Company Name: astellas pharma canada inc
Company Address: 675 Cochrane Drive, West Tower, Suite 650, Markham, Ontario, Canada, L3R 0B8

Active Ingredients

FEZOLINETANT

45 MG

Authorized

Quick Info

Agency

Health Canada

Country

🇨🇦

Approval Date

Jul 4, 2025

Approval ID

1fa88d0fb5be6931

Type

Standard

Back to Health Canada Approvals