Approvals/CIMA-AEMPS/VORICONAZOL HIKMA 200 MG POLVO PARA SOLUCION PARA PERFUSION EFG

Approved

STANDARD

VORICONAZOL HIKMA 200 MG POLVO PARA SOLUCION PARA PERFUSION EFG

Hikma Farmaceutica (Portugal) S.A.🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Id: 28fbd80d036defb4
Drug Cima Aemps Name: VORICONAZOL HIKMA 200 MG POLVO PARA SOLUCION PARA PERFUSION EFG
Register Number: 1151004001
Holder Company Name: Hikma Farmaceutica (Portugal) S.A.
Marketing Company Name: Hikma España, S.L.U.
Holder Company Detail Path: /organization/hikma-farmaceutica-portugal-s-a
Authorization Date: 2022-01-31
Dosage Form: POLVO PARA SOLUCIÓN PARA PERFUSIÓN
Dose: 200 mg
Route Of Administration: VÍA INTRAVENOSA
Prescription Type: Uso Hospitalario
Commercialized: Yes
Company Name: Hikma Farmaceutica (Portugal) S.A.
Company Detail Path: /organization/hikma-farmaceutica-portugal-s-a

VORICONAZOL

200 mg

Approved

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Jan 31, 2022

Approval ID

28fbd80d036defb4

Type

Standard