SOOLANTRA

This brand name is authorized in Austria, Brazil, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Ireland, Israel, Lithuania, Malta, Netherlands, Poland, Romania, Singapore, Tunisia, Turkey, United Kingdom, United States

Active ingredients

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

1 Ivermectin
UNII 8883YP2R6D - IVERMECTIN

Ivermectin is a member of the avermectin class and has high affinity with glutamate-gated chloride channels present in invertebrate nerve and muscle cells. Its binding to these channels promotes an increase in membrane permeability to chloride ions, leading to hyperpolarization of the neural or muscle cell. This results in neuromuscular paralysis and may lead to the death of certain parasites.

Read about Ivermectin

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
SOOLANTRA Cream Medicines & Healthcare Products Regulatory Agency (GB) 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
D11AX22 D Dermatologicals → D11 Other dermatological preparations → D11A Other dermatological preparations → D11AX Other dermatologicals
Discover more medicines within D11AX22

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): 510120070005907
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 4549-MEE-0119
Country: EE Ravimiamet Identifier(s): 1644724, 1644735, 1644746, 1644757, 1644768
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 79911
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 058790, 119528
Country: FR Base de données publique des médicaments Identifier(s): 69444281
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 297364
Country: HK Department of Health Drug Office Identifier(s): 64980
Country: IE Health Products Regulatory Authority Identifier(s): 38602, 38693
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 8790, 8791, 8946
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1073154, 1076602, 1076603, 1076604, 1076605
Country: MT Medicines Authority Identifier(s): MA117/01101
Country: NL Z-Index G-Standaard Identifier(s): 16211286
Country: NL Z-Index G-Standaard, PRK Identifier(s): 129674
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100341880
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W61758001, W61758002, W61758003, W61758004, W61758005
Country: SG Health Sciences Authority Identifier(s): 15197P
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 7393121
Country: TR İlaç ve Tıbbi Cihaz Kurumu Identifier(s): 8680530820136
Country: US FDA, National Drug Code Identifier(s): 0299-3823

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