Approvals/CIMA-AEMPS/VORICONAZOL SEACROSS 200 MG POLVO PARA SOLUCIÓN PARA PERFUSIÓN EFG

Approved

STANDARD

VORICONAZOL SEACROSS 200 MG POLVO PARA SOLUCIÓN PARA PERFUSIÓN EFG

Seacross Pharma (Europe) Limited🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Id: d083e489b0dd88e3
Drug Cima Aemps Name: VORICONAZOL SEACROSS 200 MG POLVO PARA SOLUCIÓN PARA PERFUSIÓN EFG
Register Number: 90020
Holder Company Name: Seacross Pharma (Europe) Limited
Marketing Company Name: Pharmavic Iberica S.L.
Authorization Date: 2024-12-16
Dosage Form: POLVO PARA SOLUCIÓN PARA PERFUSIÓN
Dose: 200 mg
Route Of Administration: VÍA INTRAVENOSA
Prescription Type: Uso Hospitalario
Commercialized: Yes
Company Name: Seacross Pharma (Europe) Limited

VORICONAZOL

200 mg

Approved

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Dec 16, 2024

Approval ID

d083e489b0dd88e3

Type

Standard