FLUARIX TETRA

This brand name is authorized in Austria, Brazil, Estonia, Spain, Finland, Hong Kong, Ireland, Israel, Lithuania, Malta, New Zealand, Poland, Singapore, Turkey, United Kingdom

Active ingredients

The drug FLUARIX TETRA contains a combination of these active pharmaceutical ingredients (APIs):

1 A/Victoria/4897/2022 (H1N1)pdm09-like strain (A/Victoria/4897/2022, IVR-238)
Read about Influenza, inactivated, split virus
2 A/Darwin/9/2021 (H3N2)-like strain (A/Darwin/6/2021, IVR-227)
Read about Influenza, inactivated, split virus
3 B/Austria/1359417/2021-like strain (B/Austria/1359417/2021, BVR-26)
Read about Influenza, inactivated, split virus
4 B/Phuket/3073/2013-like strain (B/Phuket/3073/2013, wild type)
Read about Influenza, inactivated, split virus

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC code Group title Classification
J07BB02 Influenza, purified antigen J Antiinfectives for systemic use → J07 Vaccines → J07B Viral vaccines → J07BB Influenza vaccines
Discover more medicines within J07BB02

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 510615110054302, 510615110054402
Country: EE Ravimiamet Identifier(s): 1763850, 1763861
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 78568
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 507366, 517806
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 252565
Country: HK Department of Health Drug Office Identifier(s): 62234, 62235, 63226
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 7676
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1085809, 1085810, 1085811, 1085812, 1085813
Country: MT Medicines Authority Identifier(s): MA170/01101
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 16664
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100402273
Country: SG Health Sciences Authority Identifier(s): 14760P
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699522964413, 8699522964437

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