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Thiothixene

Prescription ANDA TE AB Official labelling
Informational index, not medical advice. Content is reproduced from public FDA and NLM data. Always confirm against the manufacturer's current prescribing information. Report adverse events to FDA MedWatch.

Overview

Brand name
Thiothixene
Generic name
Thiothixene
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA
Labeler
Amneal Pharmaceuticals NY LLC
Product type
Human Prescription Drug
DEA schedule
Not scheduled
Active ingredients
4
NDC product codes
13
Packages
24
Data completeness
82% of corroborating sources present

Active ingredients

Source: NDC Directory
Active ingredients and strengths as listed in the NDC Directory.
Ingredient Strength RxCUI Monograph
Thiothixene 1 mg/1 313361 —
Thiothixene 10 mg/1 313361 —
Thiothixene 2 mg/1 313361 —
Thiothixene 5 mg/1 313361 —

Forms, strengths and routes

Source: NDC Directory
Dosage form
Capsule
Route of administration
Oral
Presentations
37

Pharmacologic classes are listed in the class section below.

Pharmacologic class

Source: NDC Directory
Established pharmacologic classes (EPC), mechanisms of action (MoA), chemical structures (CS) and physiologic effects (PE).
Class Type Browse
Typical Antipsychotic [EPC] EPC All 10 members

Regulatory status

Source: Drugs@FDANDC Directory
Application number
211642
Application type
ANDA · Abbreviated New Drug Application
Approval date
April 5, 2019
Sponsor
NOVITIUM PHARMA
Products on application
4
Submissions recorded
2
Products approved under application 211642.
Product Trade name Form Strength Ingredient Status TE Flags
211642-001 THIOTHIXENE CAPSULE THIOTHIXENE Prescription AB
211642-002 THIOTHIXENE CAPSULE THIOTHIXENE Prescription AB
211642-003 THIOTHIXENE CAPSULE THIOTHIXENE Prescription AB RS
211642-004 THIOTHIXENE CAPSULE THIOTHIXENE Prescription AB

Therapeutic equivalence

Source: Orange Book
TE code
AB
Reference Listed Drug
No
Reference Standard
Yes

What this rating means: Therapeutically equivalent — bioequivalence demonstrated by in vivo or in vitro testing

Codes beginning with “A” indicate products the FDA considers therapeutically equivalent. Codes beginning with “B” indicate bioequivalence has not been established. See methodology.

Approval history

Source: Drugs@FDA
Most recent submissions on application 211642.
Type No. Action Status Date Review
Supplement 21 Labeling Approved January 22, 2025 Standard
Original application 1 Approved April 5, 2019 Standard

Review documents

  • 0 · Original application · May 22, 2019

Prescribing information

Source: openFDA Drug Labeling

Reproduced verbatim from the Structured Product Labeling submitted to the FDA (effective 20250225). This is the manufacturer's labelling text, not a summary and not advice.

HUMAN PRESCRIPTION DRUG · 20250225 HUMAN PRESCRIPTION DRUG · 20241116

Boxed Warning

openFDA Drug Labeling

BOXED WARNING WARNING 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. Analyses of seventeen placebo-controlled trials (modal duration of 10 weeks), largely in patients taking atypical antipsychotic drugs, revealed a risk of death in drug-treated patients of between 1.6 to 1.7 times the risk of death in placebo-treated patients. Over the course of a typical 10-week controlled trial, the rate of death in drug-treated patients was about 4.5%, compared to a rate of about 2.6% in the placebo group. Although the causes of death were varied, most of the deaths appeared to be either cardiovascular (e.g., heart failure, sudden death) or infectious (e.g., pneumonia) in nature. Observational studies suggest that, similar to atypical antipsychotic drugs, treatment with conventional antipsychotic drugs may increase mortality. The extent to which the findings of increased mortality in observational studies may be attributed to the antipsychotic drug as opposed to some characteristic(s) of the patients is not clear. Thiothixene is not approved for the treatment of patients with dementia-related psychosis (see WARNINGS ).

Indications and Usage

openFDA Drug Labeling

INDICATIONS & USAGE Thiothixene capsules are effective in the management of schizophrenia. Thiothixene capsules have not been evaluated in the management of behavioral complications in patients with mental retardation.

Dosage and Administration

openFDA Drug Labeling

DOSAGE AND ADMINISTRATION Dosage of thiothixene capsules should be individually adjusted depending on the chronicity and severity of the symptoms of schizophrenia. In general, small doses should be used initially and gradually increased to the optimal effective level, based on patient response. Some patients have been successfully maintained on once-a-day thiothixene capsules therapy. The use of thiothixene capsules in children under 12 years of age is not recommended because safe conditions for its use have not been established. In milder conditions, an initial dose of 2 mg three times daily is recommended. If indicated, a subsequent increase to 15 mg/day total daily dose is often effective. In more severe conditions, an initial dose of 5 mg twice daily is recommended. The usual optimal dose is 20 mg to 30 mg daily. If indicated, an increase to 60 mg/day total daily dose is often effective. Exceeding a total daily dose of 60 mg rarely increases the beneficial response.

Contraindications

openFDA Drug Labeling

CONTRAINDICATIONS Thiothixene capsules are contraindicated in patients with circulatory collapse, comatose states, central nervous system depression due to any cause, and blood dyscrasias. Thiothixene capsules are contraindicated in individuals who have shown hypersensitivity to the drug. It is not known whether there is a cross sensitivity between the thioxanthenes and the phenothiazine derivatives, but this possibility should be considered.

WARNINGS 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. Thiothixene is not approved for the treatment of patients with dementia-related psychosis (see BOXED WARNING). Tardive Dyskinesia Tardive dyskinesia, a syndrome consisting of potentially irreversible, involuntary, dyskinetic movements may develop in patients treated with antipsychotic drugs, including thiothixene (1). Although the prevalence of the syndrome appears to be highest among the elderly, especially elderly women, it is impossible to rely upon prevalence estimates to predict, at the inception of antipsychotic treatment, which patients are likely to develop the syndrome. Whether antipsychotic drug products differ in their potential to cause tardive dyskinesia is unknown. Both the risk of developing the syndrome and the likelihood that it will become irreversible are believed to increase as the duration of treatment and the total cumulative dose of antipsychotic drugs administered to the patient increase. However, the syndrome can develop, although much less commonly, after relatively brief treatment periods at low doses. There is no known treatment for established cases of tardive dyskinesia, although the syndrome may remit, partially or completely, if antipsychotic treatment is withdrawn. Antipsychotic treatment, itself, however, may suppress (or partially suppress) the signs and symptoms of the syndrome and thereby may possibly mask the underlying disease process. The effect that symptomatic suppression has upon the long-term course of the syndrome is unknown. Given these considerations, antipsychotics should be prescribed in a manner that is most likely to minimize the occurrence of tardive dyskinesia. Chronic antipsychotic treatment should generally be reserved for patients who suffer from a chronic illness that, 1) is known to respond to antipsychotic drugs, and 2) for whom alternative, equally effective, but potentially less harmful treatments are not available or appropriate. In patients who do require chronic treatment, the smallest dose and the shortest duration of treatment producing a satisfactory clinical response should be sought. The need for continued treatment should be reassessed periodically. If signs and symptoms of tardive dyskinesia appear in a patient on antipsychotics, drug discontinuation should be considered. However, some patients may require treatment despite the presence of the syndrome. (For further information about the description of tardive dyskinesia and its clinical detection, please refer to Information for Patients in the PRECAUTIONS section, and to the ADVERSE REACTIONS section.) Neuroleptic Malignant Syndrome (NMS) A potentially fatal symptom complex sometimes referred to as Neuroleptic Malignant Syndrome (NMS) has been reported in association with antipsychotic drugs, including thiothixene 2 . Clinical manifestations of NMS are hyperpyrexia, muscle rigidity, altered mental status and evidence of autonomic instability (irregular pulse or blood pressure, tachycardia, diaphoresis, and cardiac dysrhythmias). The diagnostic evaluation of patients with this syndrome is complicated. In arriving at a diagnosis, it is important to identify cases where the clinical presentation includes both serious medical illness (e.g., pneumonia, systemic infection, etc.) and untreated or inadequately treated extrapyramidal signs and symptoms (EPS). Other important considerations in the differential diagnosis include central anticholinergic toxicity, heat stroke, drug fever and primary central nervous system (CNS) pathology. The management of NMS should include 1) immediate discontinuation of antipsychotic drugs and other drugs not essential to concurrent therapy, 2) intensive symptomatic treatment and medical monitoring, and treatment of any concomitant serious medical problems for which specific treatments a …

Adverse Reactions

openFDA Drug Labeling

ADVERSE REACTIONS NOTE : Not all of the following adverse reactions have been reported with thiothixene. However, since thiothixene has certain chemical and pharmacologic similarities to the phenothiazines, all of the known side effects and toxicity associated with phenothiazine therapy should be borne in mind when thiothixene is used. Cardiovascular Effects Tachycardia, hypotension, lightheadedness, and syncope. In the event hypotension occurs, epinephrine should not be used as a pressor agent since a paradoxical further lowering of blood pressure may result. Nonspecific EKG changes have been observed in some patients receiving thiothixene. These changes are usually reversible and frequently disappear on continued thiothixene therapy. The incidence of these changes is lower than that observed with some phenothiazines. The clinical significance of these changes is not known. CNS Effects Drowsiness, usually mild, may occur although it usually subsides with continuation of thiothixene therapy. The incidence of sedation appears similar to that of the piperazine group of phenothiazines but less than that of certain aliphatic phenothiazines. Restlessness, agitation and insomnia have been noted with thiothixene. Seizures and paradoxical exacerbation of psychotic symptoms have occurred with thiothixene infrequently. Hyperreflexia has been reported in infants delivered from mothers having received structurally related drugs. In addition, phenothiazine derivatives have been associated with cerebral edema and cerebrospinal fluid abnormalities. Extrapyramidal Symptoms Extrapyramidal symptoms, such as pseudoparkinsonism, akathisia and dystonia have been reported (see Dystonia, Class effect ). Management of these extra-pyramidal symptoms depends upon the type and severity. Rapid relief of acute symptoms may require the use of an injectable antiparkinson agent. More slowly emerging symptoms may be managed by reducing the dosage of thiothixene and/or administering an oral antiparkinson agent. Dystonia Class effect Symptoms of dystonia, prolonged abnormal contractions of muscle groups, may occur in susceptible individuals during the first few days of treatment. Dystonic symptoms include: spasm of the neck muscles, sometimes progressing to tightness of the throat, swallowing difficulty, difficulty breathing, and/or protrusion of the tongue. While these symptoms can occur at low doses, they occur more frequently and with greater severity with high potency and at higher doses of first generation antipsychotic drugs. An elevated risk of acute dystonia is observed in males and younger age groups. Persistent Tardive Dyskinesia As with all antipsychotic agents, tardive dyskinesia may appear in some patients on long-term therapy with thiothixene 1 or may occur after drug therapy has been discontinued. The syndrome is characterized by rhythmical involuntary movements of the tongue, face, mouth or jaw (e.g., protrusion of tongue, puffing of cheeks, puckering of mouth, chewing movements). Sometimes these may be accompanied by involuntary movements of extremities. Since early detection of tardive dyskinesia is important, patients should be monitored on an ongoing basis. It has been reported that fine vermicular movement of the tongue may be an early sign of the syndrome. If this or any other presentation of the syndrome is observed, the clinician should consider possible discontinuation of antipsychotic medication (see WARNINGS section). Hepatic Effects Elevations of serum transaminase and alkaline phosphatase, usually transient, have been infrequently observed in some patients. No clinically confirmed cases of jaundice attributable to thiothixene have been reported. Hematologic Effects As is true with certain other psychotropic drugs, leukopenia and leukocytosis, which are usually transient, can occur occasionally with thiothixene. Other antipsychotic drugs have been associated with agranulocytosis, eosinophilia, hemolytic anemia, thrombocytopenia and p …

Drug Interactions

openFDA Drug Labeling

DRUG INTERACTIONS Hepatic microsomal enzyme inducing agents, such as carbamazepine, were found to significantly increase the clearance of thiothixene. Patients receiving these drugs should be observed for signs of reduced thiothixene effectiveness 4,5 . Due to a possible additive effect with hypotensive agents, patients receiving these drugs should be observed closely for signs of excessive hypotension when thiothixene is added to their drug regimen 6 .

Mechanism of Action

openFDA Drug Labeling

ACTIONS Thiothixene is an antipsychotic of the thioxanthene series. Thiothixene possesses certain chemical and pharmacological similarities to the piperazine phenothiazines and differences from the aliphatic group of phenothiazines.

Description

openFDA Drug Labeling

DESCRIPTION Thiothixene is a thioxanthene derivative. Specifically, it is the cis isomer of N,N-dimethyl-9-[3-(4-methyl-1-piperazinyl)propylidene]thioxanthene-2-sulfonamide. It has a molecular formula C 23 H 29 N 3 O 2 S 2 and the molecular weight is 443.63 g/mol. The chemical structure is: The thioxanthenes differ from the phenothiazines by the replacement of nitrogen in the central ring with a carbon-linked side chain fixed in space in a rigid structural configuration. An N,N-dimethyl sulfonamide functional group is bonded to the thioxanthene nucleus. Each Thiothixene Capsules, USP contains 1 mg, 2 mg, 5 mg or 10 mg of thiothixene, USP and the following inactive ingredients: colloidal silicon dioxide, croscarmellose sodium, lactose monohydrate, magnesium stearate, microcrystalline cellulose, pregelatinized starch and sodium lauryl sulfate. Each empty hard gelatin capsule contains gelatin, iron oxide red, iron oxide yellow, purified water and titanium dioxide. In addition, the 1 mg hard gelatin capsule contains D&C yellow 10, FD&C blue 1 and FD&C red 40. The 2 mg hard gelatin capsule also contains D&C yellow 10 and ferrosoferric oxide. The 5 mg and 10 mg hard gelatin capsule also contains ferrosoferric oxide. The capsule is imprinted with black pharmaceutical ink which contains ferrosoferric oxide, potassium hydroxide, propylene glycol and shellac. structure

OVERDOSAGE Manifestations include muscular twitching, drowsiness and dizziness. Symptoms of gross overdosage may include CNS depression, rigidity, weakness, torticollis, tremor, salivation, dysphagia, hypotension, disturbances of gait, or coma. Treatment Essentially symptomatic and supportive. Early gastric lavage is helpful. Keep patient under careful observation and maintain an open airway, since involvement of the extrapyramidal system may produce dysphagia and respiratory difficulty in severe overdosage. If hypotension occurs, the standard measures for managing circulatory shock should be used (intravenous (I.V.) fluids and/or vasoconstrictors). If a vasoconstrictor is needed, levarterenol and phenylephrine are the most suitable drugs. Other pressor agents, including epinephrine, are not recommended, since phenothiazine derivatives may reverse the usual pressor action of these agents and cause further lowering of blood pressure. If CNS depression is marked, symptomatic treatment is indicated. Extrapyramidal symptoms may be treated with antiparkinson drugs. There are no data on the use of peritoneal or hemodialysis, but they are known to be of little value in phenothiazine intoxication.

How Supplied / Storage and Handling

openFDA Drug Labeling

HOW SUPPLIED Thiothixene Capsules, USP are available containing 1 mg, 2 mg, 5 mg or 10 mg of thiothixene, USP. Thiothixene, USP 1 mg capsule is a size 4 hard gelatin capsule with a caramel opaque cap and a blue opaque body filled with white to off-white powder. The capsule is imprinted “014” on the cap and “novitium” on the body in black ink. They are available as below: NDC 70954-014-10 Bottle of 100 capsules NDC 70954-014-20 Bottle of 1000 capsules Thiothixene, USP 2 mg capsule is a size 4 hard gelatin capsule with a caramel opaque cap and a yellow opaque body filled with white to off-white powder. The capsule is imprinted “015” on the cap and “novitium” on the body in black ink. They are available as below: NDC 70954-015-10 Bottle of 100 capsules NDC 70954-015-20 Bottle of 1000 capsules NDC 70954-015-40 Unit dose blister packages of 100 (10 cards of 10 capsules each) Thiothixene, USP 5 mg capsule is a size 4 hard gelatin capsule with a caramel opaque cap and a white opaque body filled with white to off-white powder. The capsule is imprinted “016” on the cap and “novitium” on the body in black ink. They are available as below: NDC 70954-016-10 Bottle of 100 capsules NDC 70954-016-20 Bottle of 1000 capsules NDC 70954-016-40 Unit dose blister packages of 100 (10 cards of 10 capsules each) Thiothixene, USP 10 mg capsule is a size 4 hard gelatin capsule with a caramel opaque cap and a peach opaque body filled with white to off-white powder. The capsule is imprinted “017” on the cap and “novitium” on the body in black ink. They are available as below: NDC 70954-017-10 Bottle of 100 capsules NDC 70954-017-20 Bottle of 1000 capsules NDC 70954-017-40 Unit dose blister packages of 100 (10 cards of 10 capsules each) Store at 20° to 25°C (68° to 77°F). [See USP Controlled Room Temperature.] Protect from light. Preserve in tight, light-resistant container as defined in the USP.

Adverse event reports

Source: openFDA FAERS
217
FAERS reports mentioning this drug
as of 2026-09-25T03:42:24+00:00
A report count is not a risk measure. FAERS accepts voluntary and mandatory reports without establishing causation, and reporting is influenced by how widely a drug is used, how long it has been marketed, and media attention. FDA states that reports “do not prove that the drug caused the event”. Compare rates, not totals.

Attributed to this product's most-reported active ingredient: THIOTHIXENE. Combination products with more than six active ingredients are not attributed, because a report count summed across a long ingredient list measures the list, not the medicine.

Packaging and NDCs

Source: NDC Directory
Every National Drug Code package associated with this medication. The NDC is the identifier used for dispensing, billing and pharmacovigilance in the United States.
Package NDC Product NDC Labeler Description Marketing start
70954-014-10 70954-014 ANI Pharmaceuticals, Inc. 100 CAPSULE in 1 BOTTLE (70954-014-10) April 5, 2019
70954-014-20 70954-014 ANI Pharmaceuticals, Inc. 1000 CAPSULE in 1 BOTTLE (70954-014-20) April 5, 2019
70954-015-10 70954-015 ANI Pharmaceuticals, Inc. 100 CAPSULE in 1 BOTTLE (70954-015-10) April 5, 2019
70954-015-20 70954-015 ANI Pharmaceuticals, Inc. 1000 CAPSULE in 1 BOTTLE (70954-015-20) April 5, 2019
70954-015-40 70954-015 ANI Pharmaceuticals, Inc. 100 BLISTER PACK in 1 CARTON (70954-015-40) / 1 CAPSULE in 1 BLISTER PACK (70954-015-30) August 28, 2020
70954-016-10 70954-016 ANI Pharmaceuticals, Inc. 100 CAPSULE in 1 BOTTLE (70954-016-10) April 5, 2019
70954-016-20 70954-016 ANI Pharmaceuticals, Inc. 1000 CAPSULE in 1 BOTTLE (70954-016-20) April 5, 2019
70954-016-40 70954-016 ANI Pharmaceuticals, Inc. 100 BLISTER PACK in 1 CARTON (70954-016-40) / 1 CAPSULE in 1 BLISTER PACK (70954-016-30) August 28, 2020
70954-017-10 70954-017 ANI Pharmaceuticals, Inc. 100 CAPSULE in 1 BOTTLE (70954-017-10) April 5, 2019
70954-017-20 70954-017 ANI Pharmaceuticals, Inc. 1000 CAPSULE in 1 BOTTLE (70954-017-20) April 5, 2019
70954-017-40 70954-017 ANI Pharmaceuticals, Inc. 100 BLISTER PACK in 1 CARTON (70954-017-40) / 1 CAPSULE in 1 BLISTER PACK (70954-017-30) August 28, 2020
60219-1673-1 60219-1673 Amneal Pharmaceuticals NY LLC 100 CAPSULE in 1 BOTTLE, PLASTIC (60219-1673-1) March 3, 2022
60219-1673-7 60219-1673 Amneal Pharmaceuticals NY LLC 1000 CAPSULE in 1 BOTTLE, PLASTIC (60219-1673-7) March 3, 2022
60219-1674-1 60219-1674 Amneal Pharmaceuticals NY LLC 100 CAPSULE in 1 BOTTLE, PLASTIC (60219-1674-1) March 3, 2022
60219-1674-7 60219-1674 Amneal Pharmaceuticals NY LLC 1000 CAPSULE in 1 BOTTLE, PLASTIC (60219-1674-7) March 3, 2022
60219-1675-1 60219-1675 Amneal Pharmaceuticals NY LLC 100 CAPSULE in 1 BOTTLE, PLASTIC (60219-1675-1) March 3, 2022
60219-1675-7 60219-1675 Amneal Pharmaceuticals NY LLC 1000 CAPSULE in 1 BOTTLE, PLASTIC (60219-1675-7) March 3, 2022
60219-1676-1 60219-1676 Amneal Pharmaceuticals NY LLC 100 CAPSULE in 1 BOTTLE, PLASTIC (60219-1676-1) March 3, 2022
60219-1676-7 60219-1676 Amneal Pharmaceuticals NY LLC 1000 CAPSULE in 1 BOTTLE, PLASTIC (60219-1676-7) March 3, 2022
67046-1542-3 67046-1542 Coupler LLC 30 CAPSULE in 1 BLISTER PACK (67046-1542-3) March 26, 2025
51407-275-01 51407-275 Golden State Medical Supply, Inc. 100 CAPSULE in 1 BOTTLE (51407-275-01) August 20, 2019
51407-276-01 51407-276 Golden State Medical Supply, Inc. 100 CAPSULE in 1 BOTTLE (51407-276-01) August 20, 2019
51407-277-01 51407-277 Golden State Medical Supply, Inc. 100 CAPSULE in 1 BOTTLE (51407-277-01) August 20, 2019
51407-278-01 51407-278 Golden State Medical Supply, Inc. 100 CAPSULE in 1 BOTTLE (51407-278-01) August 20, 2019
70954-014 70954-014 ANI Pharmaceuticals, Inc. — April 5, 2019
70954-015 70954-015 ANI Pharmaceuticals, Inc. — April 5, 2019
70954-016 70954-016 ANI Pharmaceuticals, Inc. — April 5, 2019
70954-017 70954-017 ANI Pharmaceuticals, Inc. — April 5, 2019
60219-1673 60219-1673 Amneal Pharmaceuticals NY LLC — March 3, 2022
60219-1674 60219-1674 Amneal Pharmaceuticals NY LLC — March 3, 2022
60219-1675 60219-1675 Amneal Pharmaceuticals NY LLC — March 3, 2022
60219-1676 60219-1676 Amneal Pharmaceuticals NY LLC — March 3, 2022
67046-1542 67046-1542 Coupler LLC — March 26, 2025
51407-275 51407-275 Golden State Medical Supply, Inc. — April 5, 2019
51407-276 51407-276 Golden State Medical Supply, Inc. — April 5, 2019
51407-277 51407-277 Golden State Medical Supply, Inc. — April 5, 2019
51407-278 51407-278 Golden State Medical Supply, Inc. — April 5, 2019

Sources for this page

Every dataset that contributed a fact to this page.
Dataset Agency Used for
NDC Directory FDA Identity, ingredients, strengths, forms, routes, labelers, packages
Drugs@FDA FDA Application, sponsor, submissions, review documents, marketing status
Orange Book FDA Therapeutic equivalence codes, reference drug flags, patents, exclusivity
Drug Labeling FDA / NLM Prescribing information reproduced above
FAERS FDA Adverse event report counts

Generated September 25, 2026 · 11 sections on this page.