This brand name is authorized in Austria, Canada, Croatia, Finland, France, Hong Kong SAR China, Ireland, Israel, Netherlands, New Zealand, Poland, Romania, Turkey.
The drug ACARIZAX contains a combination of these active pharmaceutical ingredients (APIs):
1
|
Dermatophagoides farinae allergen extract
UNII
PR9U2YPF3Q - DERMATOPHAGOIDES FARINAE
|
2
|
Dermatophagoides pteronyssinus allergen extract
UNII
57L1Z5378K - DERMATOPHAGOIDES PTERONYSSINUS
|
Below package inserts are available for further reading:
Document | Type | Information Source | |
---|---|---|---|
ACARIZAX Oral lyophilisate | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
ATC Group | Classification | |
---|---|---|
V01AA03 | House dust | V Various → V01 Allergens → V01A Allergens → V01AA Allergen extracts |
This drug has been assigned below unique identifiers within the countries it is being marketed:
Country | Identification scheme | Identifier(s) |
---|---|---|
CA | Health Products and Food Branch | 02463644 |
FI | Lääkealan turvallisuus- ja kehittämiskeskus | 186748, 555047 |
FR | Base de données publique des médicaments | 67813445 |
HK | Department of Health Drug Office | 65924 |
HR | Agencija za lijekove i medicinske proizvode | HR-H-514558232 |
IL | מִשְׂרַד הַבְּרִיאוּת | 8808 |
NL | Z-Index G-Standaard, PRK | 205400 |
NZ | Medicines and Medical Devices Safety Authority | 18800 |
PL | Rejestru Produktów Leczniczych | 100330160 |
RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W67212001, W67212002, W67212003 |
TR | İlaç ve Tıbbi Cihaz Kurumu | 8681078093945, 8681078093952, 8681078093969 |
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