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NUVAXOVID XBB.1.5 DISPERSION INYECTABLE - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
NUVAXOVID XBB.1.5 DISPERSION INYECTABLE
Approved
STANDARD
NUVAXOVID XBB.1.5 DISPERSION INYECTABLE
Sanofi Winthrop Industrie
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Nov 20, 2023
Approval ID
09be04df3a480db6
Company
Sanofi Winthrop Industrie
Type
Standard
Approval Details
Approval Id
09be04df3a480db6
Drug Cima Aemps Name
NUVAXOVID XBB.1.5 DISPERSION INYECTABLE
Register Number
1211618008
Holder Company Name
Sanofi Winthrop Industrie
Marketing Company Name
Sanofi Aventis S.A.
Holder Company Detail Path
/organization/sanofi-winthrop-industrie
Authorization Date
2023-11-20
Dosage Form
DISPERSIÓN INYECTABLE
Dose
5 MICROGRAMOS
Route Of Administration
VÍA INTRAMUSCULAR
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
No
Company Name
Sanofi Winthrop Industrie
Company Detail Path
/organization/sanofi-winthrop-industrie
Company Information
Pharmaceutical Company Name
SANOFI WINTHROP INDUSTRIE
Country Name
France
City Name
amilly,centre val de loire,country_fr
Address
130 RUE DE LA FONTAINE
Active Ingredients
VACUNA DE PROTEINA RECOMBINANTE DE LA ESPICULA DE SARS-COV-2 (OMICRON XBB.1.5)(NOVAVAX)
5 µg/dosis
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Nov 20, 2023
Approval ID
09be04df3a480db6
Type
Standard
Back to CIMA-AEMPS Approvals