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COMIRNATY ORIGINAL/OMICRON BA.4-5 (5/5 MICROGRAMOS)/DOSIS CONCENTRADO PARA DISPERSION INYECTABLE - CIMA-AEMPS Drug Approval Details
Approvals
/
CIMA-AEMPS
/
COMIRNATY ORIGINAL/OMICRON BA.4-5 (5/5 MICROGRAMOS)/DOSIS CONCENTRADO PARA DISPERSION INYECTABLE
Approved
STANDARD
COMIRNATY ORIGINAL/OMICRON BA.4-5 (5/5 MICROGRAMOS)/DOSIS CONCENTRADO PARA DISPERSION INYECTABLE
Biontech Manufacturing Gmbh
🇪🇸 Spanish Agency of Medicines and Medical Devices
Approval Date
Nov 17, 2022
Approval ID
6e34b76433b54cfe
Company
Biontech Manufacturing Gmbh
Type
Standard
Approval Details
Approval Id
6e34b76433b54cfe
Drug Cima Aemps Name
COMIRNATY ORIGINAL/OMICRON BA.4-5 (5/5 MICROGRAMOS)/DOSIS CONCENTRADO PARA DISPERSION INYECTABLE
Register Number
1201528011
Holder Company Name
Biontech Manufacturing Gmbh
Marketing Company Name
Pfizer S.L.
Holder Company Detail Path
/organization/biontech-manufacturing-gmbh
Authorization Date
2022-11-17
Dosage Form
CONCENTRADO PARA DISPERSION INYECTABLE
Dose
0,2 ML
Route Of Administration
VÍA INTRAMUSCULAR
Prescription Type
Medicamento Sujeto A Prescripción Médica
Commercialized
No
Company Name
Biontech Manufacturing Gmbh
Company Detail Path
/organization/biontech-manufacturing-gmbh
Company Information
Pharmaceutical Company Name
BioNTech Manufacturing GmbH
Country Name
Germany
Active Ingredients
TOZINAMERAN
0,05 mg/ml
FAMTOZINAMERAN
0,05 mg/ml
Approved
Quick Info
Agency
CIMA-AEMPS
Country
🇪🇸
Approval Date
Nov 17, 2022
Approval ID
6e34b76433b54cfe
Type
Standard
Back to CIMA-AEMPS Approvals