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/CIMA-AEMPS/ZONISAMIDA AUROVITAS 50 MG CAPSULAS DURAS EFG

Approved

STANDARD

ZONISAMIDA AUROVITAS 50 MG CAPSULAS DURAS EFG

Aurovitas Spain, S.A.U.🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: May 9, 2022
Approval ID: f533e4958bebc9fd
Company: Aurovitas Spain, S.A.U.
Type: Standard

Approval Details

Approval Id: f533e4958bebc9fd
Drug Cima Aemps Name: ZONISAMIDA AUROVITAS 50 MG CAPSULAS DURAS EFG
Register Number: 87157
Holder Company Name: Aurovitas Spain, S.A.U.
Marketing Company Name: Aurovitas Spain, S.A.U.
Authorization Date: 2022-05-09
Dosage Form: CÁPSULA DURA
Dose: 50 mg
Route Of Administration: VÍA ORAL
Prescription Type: Medicamento Sujeto A Prescripción Médica
Commercialized: Yes
Company Name: Aurovitas Spain, S.A.U.

Active Ingredients

ZONISAMIDA

50 mg

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

May 9, 2022

Approval ID

f533e4958bebc9fd

Type

Standard

Back to CIMA-AEMPS Approvals

ZONISAMIDA AUROVITAS 50 MG CAPSULAS DURAS EFG - CIMA-AEMPS Drug Approval Details