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VANFLYTA 17,7 MG COMPRIMIDOS RECUBIERTOS CON PELICULA - CIMA-AEMPS Drug Approval Details

Approvals/CIMA-AEMPS/VANFLYTA 17,7 MG COMPRIMIDOS RECUBIERTOS CON PELICULA

Approved

STANDARD

VANFLYTA 17,7 MG COMPRIMIDOS RECUBIERTOS CON PELICULA

Daiichi Sankyo Europe Gmbh🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: Mar 19, 2024
Approval ID: 2434a7dede7775fd
Company: Daiichi Sankyo Europe Gmbh
Type: Standard

Approval Details

Approval Id: 2434a7dede7775fd
Drug Cima Aemps Name: VANFLYTA 17,7 MG COMPRIMIDOS RECUBIERTOS CON PELICULA
Register Number: 1231768002
Holder Company Name: Daiichi Sankyo Europe Gmbh
Marketing Company Name: Daiichi Sankyo Espana S.A.
Holder Company Detail Path: /organization/daiichi-sankyo-europe-gmbh
Authorization Date: 2024-03-19
Dosage Form: COMPRIMIDO RECUBIERTO CON PELÍCULA
Dose: 17,7 mg
Route Of Administration: VÍA ORAL
Prescription Type: Diagnóstico Hospitalario
Commercialized: Yes
Company Name: Daiichi Sankyo Europe Gmbh
Company Detail Path: /organization/daiichi-sankyo-europe-gmbh

Company Information

Pharmaceutical Company Name: Daiichi Sankyo Europe GmbH
Country Name: Germany
City Name: münchen,bayern,country_de
Address: Zielstattstr. 48
Website: http://www.daiichi-sankyo.eu

Active Ingredients

QUIZARTINIB DIHIDROCLORURO

17,7 mg

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Mar 19, 2024

Approval ID

2434a7dede7775fd

Type

Standard

Back to CIMA-AEMPS Approvals