KANJINTI

This brand name is authorized in Austria, Australia, Brazil, Canada, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Lithuania, Netherlands, New Zealand, Poland, Romania, Turkey, United Kingdom, United States

Active ingredients

The drug KANJINTI contains one active pharmaceutical ingredient (API):

1 Trastuzumab
UNII P188ANX8CK - TRASTUZUMAB

Trastuzumab is a recombinant humanised IgG1 monoclonal antibody against the human epidermal growth factor receptor 2 (HER2). Τrastuzumab has been shown, in both in vitro assays and in animals, to inhibit the proliferation of human tumour cells that overexpress HER2.

Read about Trastuzumab

Medicine classification

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

ATC code Group title Classification
L01FD01 Trastuzumab L Antineoplastic and immunomodulating agents → L01 Antineoplastic agents → L01F Monoclonal antibodies and antibody drug conjugates → L01FD HER2 (Human Epidermal Growth Factor Receptor 2) inhibitors
Discover more medicines within L01FD01

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 10383L, 10391X, 10401K, 10402L, 10581X, 10588G, 10589H, 10597R, 4632T, 4639E, 4650R, 4703M, 7264H, 7265J, 7266K, 7267L
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 544120010004807, 544120010004907, 544120010005007
Country: CA Health Products and Food Branch Identifier(s): 02496690
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 192-MBE-0421, 205-MBE-0621
Country: EE Ravimiamet Identifier(s): 1773019, 1773020
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 1181281001, 1181281002
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 177924
Country: FR Base de données publique des médicaments Identifier(s): 61193788, 61529324
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 355528, 358910
Country: HK Department of Health Drug Office Identifier(s): 66599, 66628
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8971
Country: IT Agenzia del Farmaco Identifier(s): 046547016, 046547028
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1085605, 1085606
Country: NL Z-Index G-Standaard, PRK Identifier(s): 150975, 57991
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 20782, 20783, 20784
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100406325, 100406331
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W65029001, W65030001
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8699862270038
Country: US FDA, National Drug Code Identifier(s): 55513-132, 55513-141

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