IMODIUM

This brand name is authorized in Austria, Canada, Cyprus, Germany, Estonia, Finland, France, Hong Kong, Croatia, Ireland, Israel, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, United Kingdom, South Africa

Active ingredients

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

1 Loperamide
UNII 77TI35393C - LOPERAMIDE HYDROCHLORIDE

By binding to opiate receptors in the gut wall, loperamide hydrochloride reduces propulsive peristalsis, increases intestinal transit time and enhances resorption of water and electrolytes. Loperamide increases the tone of the anal sphincter, which helps reduce faecal incontinence and urgency.

Read about Loperamide

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
IMODIUM Capsule Health Products Regulatory Authority (IE) 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
A07DA03 Loperamide A Alimentary tract and metabolism → A07 Antidiarrheals, intestinal antiinflammatory/antiinfective agents → A07D Antipropulsives → A07DA Antipropulsives
Discover more medicines within A07DA03

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: CA Health Products and Food Branch Identifier(s): 02230542, 02291800, 02376016
Country: DE Bundesinstitut für Arzneimittel und Medizinprodukte Identifier(s): 00141551, 01689848, 01689854, 01869444, 02334188, 03829609, 04638834, 04910153, 04910176, 04940757, 07296788, 07299261, 07370740, 07374293, 07606533
Country: EE Ravimiamet Identifier(s): 1008997, 1063482, 1603651, 1603662, 1603673
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 037669, 080755, 497499, 569277, 569285
Country: FR Base de données publique des médicaments Identifier(s): 60095095, 61203061, 61651634, 65272215, 69522794
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 18234, 185535, 185536, 19243, 279804, 279805, 289618, 299082, 299083, 81424
Country: HK Department of Health Drug Office Identifier(s): 46489
Country: IE Health Products Regulatory Authority Identifier(s): 28681, 28706
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 3220
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1008165, 1015752, 1022765, 1068119, 1069908, 1076666
Country: MT Medicines Authority Identifier(s): AA565/73301, AA908/06503, MA1471/00301, PI521/01801C, PI908/06501A
Country: MX Comisión Federal para la Protección contra Riesgos Sanitarios Identifier(s): 83335
Country: NL Z-Index G-Standaard Identifier(s): 12310700
Country: NL Z-Index G-Standaard, PRK Identifier(s): 15695, 3212, 85391
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 11324, 14818, 15626, 15627
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100105204
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W64913001, W64913002, W65625001, W65625002, W65625003, W65625004
Country: SG Health Sciences Authority Identifier(s): 06212P
Country: ZA Health Products Regulatory Authority Identifier(s): 29/11.9/0213, H/11.9/152, J/11.9/166, U/11.9/213

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