LOCERYL

This brand name is authorized in Australia, Austria, Brazil, Cyprus, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Lithuania, Malta, New Zealand, Poland, Singapore, South Africa, Tunisia, Turkey, UK.

Active ingredients

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

1	Amorolfine UNII 741YH7379H - AMOROLFINE HYDROCHLORIDE
	Amorolfine is a broad spectrum antimycotic. Amorolfine belongs to a new chemical class, and its fungicidal action is based on an alteration of the fungal cell membrane targeted primarily on sterol biosynthesis. The ergosterol content is reduced, and at the same time unusual sterically nonplanar sterols accumulate.
	Read more about Amorolfine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
LOCERYL Nail lacquer	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group		Classification
D01AE16	Amorolfine	D Dermatologicals → D01 Antifungals for dermatological use → D01A Antifungals for topical use → D01AE Other antifungals for topical use
Discover more medicines within D01AE16

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
AU	Pharmaceutical Benefits Scheme	4010C
BR	Câmara de Regulação do Mercado de Medicamentos	510100901165319, 510114110005703, 510115030005903, 510119010006103
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	25.598-03-04
EE	Ravimiamet	1009572, 1009842, 1061042, 1740866, 1740877, 1742015, 1742026, 1860555
FI	Lääkealan turvallisuus- ja kehittämiskeskus	049551, 176955
FR	Base de données publique des médicaments	65581507, 66895425
GB	Medicines & Healthcare Products Regulatory Agency	103552, 22885
HK	Department of Health Drug Office	36522, 51795
IE	Health Products Regulatory Authority	31437, 31457, 31462
IL	מִשְׂרַד הַבְּרִיאוּת	6003
LT	Valstybinė vaistų kontrolės tarnyba	1012309, 1070286, 1078453, 1088352, 1088353, 1088642, 1088643, 1088691, 1089625, 1090866, 1093402
MT	Medicines Authority	MA117/00401
NZ	Medicines and Medical Devices Safety Authority	6146
PL	Rejestru Produktów Leczniczych	100039460, 100189000, 100339830, 100359376, 100398838
SG	Health Sciences Authority	07506P
TN	Direction de la Pharmacie et du Médicament	7393061
TR	İlaç ve Tıbbi Cihaz Kurumu	8699586652622
ZA	Health Products Regulatory Authority	27/13.9.2/0163