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HEMLIBRA 150 MG/ML SOLUCION INYECTABLE - CIMA-AEMPS Drug Approval Details

Approvals/CIMA-AEMPS/HEMLIBRA 150 MG/ML SOLUCION INYECTABLE

Approved

STANDARD

HEMLIBRA 150 MG/ML SOLUCION INYECTABLE

Roche Registration Gmbh🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: Nov 3, 2025
Approval ID: 65e696d3c61675e6
Company: Roche Registration Gmbh
Type: Standard

Approval Details

Approval Id: 65e696d3c61675e6
Drug Cima Aemps Name: HEMLIBRA 150 MG/ML SOLUCION INYECTABLE
Register Number: 1181271002IP2
Holder Company Name: Roche Registration Gmbh
Marketing Company Name: Orifarm A/S
Holder Company Detail Path: /organization/roche-registration-gmbh
Authorization Date: 2025-11-03
Dosage Form: SOLUCIÓN INYECTABLE
Dose: 150 mg/ml
Route Of Administration: VÍA SUBCUTÁNEA
Prescription Type: Diagnóstico Hospitalario
Commercialized: No
Company Name: Roche Registration Gmbh
Company Detail Path: /organization/roche-registration-gmbh

Company Information

Pharmaceutical Company Name: Roche Registration GmbH
Country Name: Germany
City Name: grenzach-wyhlen,baden-württemberg,country_de
Address: Emil-Barell-Str. 1

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Nov 3, 2025

Approval ID

65e696d3c61675e6

Type

Standard

Back to CIMA-AEMPS Approvals