ATC (Anatomical Therapeutic Chemical Classification)
CAS registry number (Chemical Abstracts Service)
Enzyme replacement therapy
α-Galactosidase (human clone, tAG¹⁸ isoenzyme A subunit protein moiety reduced) (USAN)
Human alpha-galactosidase isoenzyme A, isolated from human cell line, clone RAG 001, glycoform α (WHO)
- Agalsidasum alfa (Latin)
- Agalsidase alfa (German)
- Agalsidase alfa (French)
- Agalsidasa alfa (Spanish)
- Agalsidase Alfa (OS: USAN, BAN)
- Agalsidase Alfa (Genetical Recombination) (OS: JAN)
- Alpha-galactosidase (IS)
- EC 22.214.171.124. (IS)
Genzyme, Thailand; Sanofi-Aventis, Bosnia & Herzegowina; Sanofi-Aventis, Thailand
DRAC, Switzerland; Pharmaplan, South Africa; Shire, Australia; Shire, Belgium; Shire, Czech Republic; Shire, Spain; Shire, Finland; Shire, France; Shire, Israel; Shire, Lithuania; Shire, Netherlands; Shire, Norway; Shire, Poland; Shire, Romania; Shire, Taiwan; Shire HGT, Germany; Shire HGT, Denmark; Shire HGT, Italy; Shire Human, Greece; Shire Human Genetic Therapies, Austria; Shire Human Genetic Therapies, United Kingdom; Shire Human Genetic Therapies, Hungary; Shire Human Genetic Therapies, Sweden; Shire Human Genetic Therapies AB, Portugal; Shire Pharmaceuticals Ireland, Ireland; Solpharm, Croatia (Hrvatska)
|BAN||British Approved Name|
|JAN||Japanese Accepted Name|
|Rec.INN||Recommended International Nonproprietary Name (World Health Organization)|
|USAN||United States Adopted Name|
|WHO||World Health Organization|
Further information on drug naming conventions: International Nonproprietary Names.
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