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.

AIQLARA COMPRIMIDOS RECUBIERTOS CON PELICULA EFG - CIMA-AEMPS Drug Approval Details

Approvals/CIMA-AEMPS/AIQLARA COMPRIMIDOS RECUBIERTOS CON PELICULA EFG

Approved

STANDARD

AIQLARA COMPRIMIDOS RECUBIERTOS CON PELICULA EFG

Laboratorios Cinfa S.A.🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: Feb 19, 2025
Approval ID: 5d29a2b870dd96a8
Company: Laboratorios Cinfa S.A.
Type: Standard

Approval Details

Approval Id: 5d29a2b870dd96a8
Drug Cima Aemps Name: AIQLARA COMPRIMIDOS RECUBIERTOS CON PELICULA EFG
Register Number: 90155
Holder Company Name: Laboratorios Cinfa S.A.
Marketing Company Name: Laboratorios Cinfa S.A.
Authorization Date: 2025-02-19
Dosage Form: COMPRIMIDO RECUBIERTO CON PELÍCULA
Dose: 3 mg + 2mg/2 mg + 2 mg/3 mg + 1 mg
Route Of Administration: VÍA ORAL
Prescription Type: Medicamento Sujeto A Prescripción Médica
Commercialized: Yes
Company Name: Laboratorios Cinfa S.A.

Active Ingredients

ESTRADIOL VALERATO

2 mg

DIENOGEST

3 mg

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Feb 19, 2025

Approval ID

5d29a2b870dd96a8

Type

Standard

Back to CIMA-AEMPS Approvals