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.

IG VENA 50 G/L SOLUCION PARA PERFUSION - CIMA-AEMPS Drug Approval Details

Approvals/CIMA-AEMPS/IG VENA 50 G/L SOLUCION PARA PERFUSION

Approved

STANDARD

IG VENA 50 G/L SOLUCION PARA PERFUSION

Kedrion S.P.A.🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: Jan 27, 2023
Approval ID: d1a082bc65844fc8
Company: Kedrion S.P.A.
Type: Standard

Approval Details

Approval Id: d1a082bc65844fc8
Drug Cima Aemps Name: IG VENA 50 G/L SOLUCION PARA PERFUSION
Register Number: 88087
Holder Company Name: Kedrion S.P.A.
Marketing Company Name: Kedrion S.P.A.
Authorization Date: 2023-01-27
Dosage Form: SOLUCIÓN PARA PERFUSIÓN
Dose: 50 G/L
Route Of Administration: VÍA INTRAVENOSA
Prescription Type: Uso Hospitalario
Commercialized: Yes
Company Name: Kedrion S.P.A.

Active Ingredients

INMUNOGLOBULINA HUMANA NORMAL

50 mg

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Jan 27, 2023

Approval ID

d1a082bc65844fc8

Type

Standard

Back to CIMA-AEMPS Approvals