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Molecule

Thioridazine

Also known as thioridazine hydrochloride
Available on requestPsychiatry
Presentations
4
Brands
0
Manufacturers
0
Available from stock
0

Thioridazine is a phenothiazine indicated for the management of schizophrenic patients who fail to respond adequately to treatment with other antipsychotic drugs. It is available as tablets for oral use. MedsAcross supplies Thioridazine for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Phenothiazine
ATC classification
N05AC02 Thioridazine · Antipsychotics, subgroup N05AC
US FDA first approval
15 March 1962
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet
Identifiers
UNII N3D6TG58NIRxCUI 10502CAS 50-52-2DrugBank DB00679Q58375

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

Thioridazine hydrochloride tablets are indicated for the management of schizophrenic patients who fail to respond adequately to treatment with other antipsychotic drugs. Due to the risk of significant, potentially life threatening, proarrhythmic effects with thioridazine treatment, thioridazine hydrochloride tablets should be used only in patients who have failed to respond adequately to treatment with appropriate courses of other antipsychotic drugs, either because of insufficient effectiveness or the inability to achieve an effective dose due to intolerable adverse effects from those drugs. Consequently, before initiating treatment with thioridazine hydrochloride tablets, it is strongly recommended that a patient be given at least two trials, each with a different antipsychotic drug product, at an adequate dose, and for an adequate duration.

Source: US FDA prescribing information

Dosing overview

Since thioridazine hydrochloride tablets are associated with a dose related prolongation of the QTc interval, which is a potentially life threatening event, its use should be reserved for schizophrenic patients who fail to respond adequately to treatment with other antipsychotic drugs. Dosage must be individualized and the smallest effective dosage should be determined for each patient. Adults The usual starting dose for adult schizophrenic patients is 50 mg to 100 mg three times a day, with a gradual increment to a maximum of 800 mg daily if necessary. Once effective control of symptoms has been achieved, the dosage may be reduced gradually to determine the minimum maintenance dose. The total daily dosage ranges from 200 mg to 800 mg, divided into two to four doses.

Source: US FDA prescribing information

Contraindications

Thioridazine hydrochloride tablet use should be avoided in combination with other drugs that are known to prolong the QTc interval and in patients with congenital long QT syndrome or a history of cardiac arrhythmias. Reduced cytochrome P450 2D6 isozyme activity drugs that inhibit this isozyme (e.g., fluoxetine and paroxetine) and certain other drugs (e.g., fluvoxamine, propranolol, and pindolol) appear to appreciably inhibit the metabolism of thioridazine.

Source: US FDA prescribing information

Warnings and precautions

WARNING Thioridazine has been shown to prolong the QTc interval in a dose related manner, and drugs with this potential, including thioridazine, have been associated with Torsades de pointes type arrhythmias and sudden death. Increased Mortality in Elderly Patients with Dementia-Related Psychosis Elderly patients with dementia-related psychosis treated with antipsychotic drugs are at an increased risk of death. Thioridazine hydrochloride is not approved for the treatment of patients with dementia-related psychosis.

Source: US FDA prescribing information

Side effects

In the recommended dosage ranges with thioridazine hydrochloride most side effects are mild and transient. Central Nervous System Drowsiness may be encountered on occasion, especially where large doses are given early in treatment. Generally, this effect tends to subside with continued therapy or a reduction in dosage. Pseudoparkinsonism and other extrapyramidal symptoms may occur but are infrequent. Nocturnal confusion, hyperactivity, lethargy, psychotic reactions, restlessness, and headache have been reported but are extremely rare. Autonomic Nervous System Dryness of mouth, blurred vision, constipation, nausea, vomiting, diarrhea, nasal stuffiness, and pallor have been seen. Endocrine System Galactorrhea, breast engorgement, amenorrhea, inhibition of ejaculation, and peripheral edema have been described.

Source: US FDA prescribing information

Interactions

Reduced cytochrome P450 2D6 isozyme activity, drugs which inhibit this isozyme (e.g., fluoxetine and paroxetine), and certain other drugs (e.g., fluvoxamine, propranolol, and pindolol) appear to appreciably inhibit the metabolism of thioridazine. The resulting elevated levels of thioridazine would be expected to augment the prolongation of the QTc interval associated with thioridazine and may increase the risk of serious, potentially fatal, cardiac arrhythmias, such as Torsades de pointes type arrhythmias. Such an increased risk may result also from the additive effect of coadministering thioridazine with other agents that prolong the QTc interval. Therefore, thioridazine is contraindicated with these drugs as well as in patients, comprising about 7% of the normal population, who are known to have a genetic defect leading to reduced levels of activity of P450 2D6.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

4 presentations of Thioridazine, sorted by availability.

MedicineManufacturerRegisterAvailability
Thioridazine 100 mg tabletOralGeneric name—US FDAAvailable on request
Thioridazine 10 mg tabletOralGeneric name—US FDAAvailable on request
Thioridazine 25 mg tabletOralGeneric name—US FDAAvailable on request
Thioridazine 50 mg tabletOralGeneric name—US FDAAvailable on request

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 15 March 1962Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Thioridazine in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Thioridazine available for export from India?

Yes, on request. MedsAcross lists 4 presentations of Thioridazine and sources them for licensed hospitals, importers and physicians against valid import documents.

Is Thioridazine approved by the US FDA?

Yes. The US FDA first approved Thioridazine on 15 March 1962, according to Drugs@FDA.

Does Thioridazine need cold chain shipping?

No listed presentation of Thioridazine is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Thioridazine in?

Thioridazine is classified under ATC code N05AC02 (Thioridazine).

References

  1. Thioridazine Hydrochloride prescribing information (Mylan Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 12 August 2026

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