KESIMPTA 20 mg SOLUCION INYECTABLE EN PLUMA PRECARGADA

Novartis Europharm Limited🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Id: c6a8716a33585320
Drug Cima Aemps Name: KESIMPTA 20 mg SOLUCION INYECTABLE EN PLUMA PRECARGADA
Register Number: 121532003
Holder Company Name: Novartis Europharm Limited
Marketing Company Name: Novartis Farmaceutica S.A.
Holder Company Detail Path: /organization/novartis-europharm-limited
Authorization Date: 2021-05-10
Dosage Form: SOLUCIÓN INYECTABLE EN PLUMA PRECARGADA
Dose: 20 mg
Route Of Administration: VÍA SUBCUTÁNEA
Prescription Type: Diagnóstico Hospitalario
Commercialized: Yes
Company Name: Novartis Europharm Limited
Company Detail Path: /organization/novartis-europharm-limited

OFATUMUMAB

20 mg

Approved

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

May 10, 2021

Approval ID

c6a8716a33585320

Type

Standard