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SHINGRIX POLVO Y SUSPENSION PARA SUSPENSION INYECTABLE - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
SHINGRIX POLVO Y SUSPENSION PARA SUSPENSION INYECTABLE
Approved
STANDARD
SHINGRIX POLVO Y SUSPENSION PARA SUSPENSION INYECTABLE
Glaxosmithkline Biologicals
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Oct 16, 2020
Approval ID
9f18859bb1fe8aeb
Company
Glaxosmithkline Biologicals
Type
Standard
Approval Details
Approval Id
9f18859bb1fe8aeb
Drug Cima Aemps Name
SHINGRIX POLVO Y SUSPENSION PARA SUSPENSION INYECTABLE
Register Number
1181272001
Holder Company Name
Glaxosmithkline Biologicals
Marketing Company Name
Glaxosmithkline S.A.
Holder Company Detail Path
/organization/glaxosmithkline-biologicals
Marketing Company Detail Path
/organization/glaxosmithkline-sa
Authorization Date
2020-10-16
Dosage Form
POLVO Y SUSPENSIÓN PARA SUSPENSIÓN INYECTABLE
Dose
50 microgramos
Route Of Administration
VÍA INTRAMUSCULAR
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
Yes
Company Name
Glaxosmithkline Biologicals
Company Detail Path
/organization/glaxosmithkline-biologicals
Company Information
Pharmaceutical Company Name
GLAXOSMITHKLINE BIOLOGICALS
Country Name
France
City Name
st amand les eaux,hauts de france,country_fr
Address
637 RUE DES AULNOIS
Active Ingredients
ANTIGENO RECOMBINANTE DE LA GLICOPROTEINA E (GE) DEL VIRUS DE LA VARICELA ZOSTER (VVZ)
50 µg
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Oct 16, 2020
Approval ID
9f18859bb1fe8aeb
Type
Standard
Back to CIMA-AEMPS Approvals