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VAXZEVRIA SUSPENSION INYECTABLE - CIMA-AEMPS Drug Approval Details

Approvals/CIMA-AEMPS/VAXZEVRIA SUSPENSION INYECTABLE

Approved

STANDARD

VAXZEVRIA SUSPENSION INYECTABLE

Astrazeneca Ab🇪🇸 Spanish Agency of Medicines and Medical Devices

Approval Date: Jan 31, 2021
Approval ID: d7bf0f80c66da517
Company: Astrazeneca Ab
Type: Standard

Approval Details

Approval Id: d7bf0f80c66da517
Drug Cima Aemps Name: VAXZEVRIA SUSPENSION INYECTABLE
Register Number: 1211529001
Holder Company Name: Astrazeneca Ab
Marketing Company Name: Astrazeneca Farmaceutica Spain S.A.
Holder Company Detail Path: /organization/astrazeneca-ab
Authorization Date: 2021-01-31
Dosage Form: SUSPENSIÓN INYECTABLE
Dose: no menos de 2,5 × 10e8 Unidades Infecciosas/0,5 ml
Route Of Administration: VÍA INTRAMUSCULAR
Prescription Type: Medicamento Sujeto A Prescripción Médica
Commercialized: No
Company Name: Astrazeneca Ab
Company Detail Path: /organization/astrazeneca-ab

Company Information

Pharmaceutical Company Name: ASTRAZENECA AB
Country Name: Spain
City Name: madrid,madrid,country_es
Address: CALLE RAIMUNDO FERNANDEZ VILLAVERDE 63
Website: http://www.astrazeneca.se

Active Ingredients

VACUNA RECOMBINANTE (CHADOX1-S) FRENTE A COVID-19 (ASTRAZENECA)

5 x 10e8 unidades infecciosas (Inf.U)

Approved

Quick Info

Agency

CIMA-AEMPS

Country

🇪🇸

Approval Date

Jan 31, 2021

Approval ID

d7bf0f80c66da517

Type

Standard

Back to CIMA-AEMPS Approvals