General Information of Drug (ID: DM1WXA6)

Drug Name
Lofexidine Drug Info
Synonyms
Britlofex; Lofexidina; Lofexidinum; Britlofex (TN); Lofexidina [INN-Spanish]; Lofexidine (INN); Lofexidine [INN:BAN]; Lofexidinum [INN-Latin]; 1H-Imidazole, 2-(1-(2,6-dichlorophenoxy)ethyl)-4,5-dihydro-(9CI); 2-(1-(2,6-Dichlorophenoxy)ethyl)-4,5-dihydro-1H-imidazole; 2-(a-(2,6-dichlorophenoxy)ethyl)2-imidazoline; 2-(alpha-(2,6-Dichlorophenoxy)ethyl)2-imidazoline; 2-(alpha-(2,6-dichlorophenoxy)ethyl) delta-2-imidazoline; 2-[1-(2,6-dichlorophenoxy)ethyl]-4,5-dihydro-1H-imidazole; 2-{1-[(2,6-dichlorophenyl)oxy]ethyl}-4,5-dihydro-1H-imidazole
Indication
Disease Entry ICD 11 Status REF
Heroin and opiate withdrawal 6C43 Approved [1]
Opioid dependence 6C43.2Z Approved [2]
Therapeutic Class
Antihypertensive Agents
Cross-matching ID
PubChem CID
30668
ChEBI ID
CHEBI:51368
CAS Number
31036-80-3
TTD ID
D0K0MW
INTEDE ID
DR0967
ACDINA ID
D01217

Full List of Drug Formulations Containing This Drug

Lofexidine 0.18 mg tablet
Company Formulation ID FDA Description
Uswm F23214 Lactose; Citric Acid; Povidone; Microcrystalline Cellulose; Calcium Stearate; Sodium Lauryl Sulphate; Indigo Carmine; Sunset Yellow
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References

1 A Phase 3 placebo-controlled, double-blind, multi-site trial of the alpha-2-adrenergic agonist, lofexidine, for opioid withdrawal. Drug Alcohol Depend. 2008 Sep 1;97(1-2):158-68.
2 2018 FDA drug approvals.Nat Rev Drug Discov. 2019 Feb;18(2):85-89.