ECALTA

This brand name is authorized in Austria, Brazil, Cyprus, Ecuador, Estonia, Spain, Finland, France, Croatia, Ireland, Lithuania, Netherlands, Poland, Romania, Tunisia, United Kingdom

Active ingredients

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

1 Anidulafungin UNII 9HLM53094I - ANIDULAFUNGIN

Anidulafungin is a semi-synthetic echinocandin, a lipopeptide synthesised from a fermentation product of Aspergillus nidulans. Anidulafungin selectively inhibits 1,3-β-D glucan synthase, an enzyme present in fungal, but not mammalian cells. Read about Anidulafungin

Medication package inserts

Below package inserts are available for further reading:

Title	Information Source	Document Type
ECALTA Powder for concentrate for solution for infusion	European Medicines Agency (EU)	MPI, EU: SmPC

Medicine classification

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

ATC code	Group title	Classification
J02AX06	Anidulafungin	J Antiinfectives for systemic use → J02 Antimycotics for systemic use → J02A Antimycotics for systemic use → J02AX Other antimycotics for systemic use
Discover more medicines within J02AX06

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): 522718020073317, 522718020073417
Country: EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	Identifier(s): 29995-09-11
Country: EE	Ravimiamet	Identifier(s): 1457041
Country: ES	Centro de información online de medicamentos de la AEMPS	Identifier(s): 07416002
Country: FI	Lääkealan turvallisuus- ja kehittämiskeskus	Identifier(s): 059644
Country: FR	Base de données publique des médicaments	Identifier(s): 60614273
Country: GB	Medicines & Healthcare Products Regulatory Agency	Identifier(s): 166379
Country: LT	Valstybinė vaistų kontrolės tarnyba	Identifier(s): 1050550
Country: NL	Z-Index G-Standaard, PRK	Identifier(s): 85448
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100180542
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W64932001
Country: TN	Direction de la Pharmacie et du Médicament	Identifier(s): 8013151H