Friday, July 10, 2026

Drug profile · INN

thiothixene hydrochloride

thiothixene hydrochloride (THIOTHIXENE HYDROCHLORIDE) is a dopamine d2 receptor antagonist. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — thiothixene hydrochloride
US status
approved
Class
Route
INJECTION
Patents
0
Programs
0
Data quality
0.89

Quick answer

thiothixene hydrochloride (THIOTHIXENE HYDROCHLORIDE) is a dopamine d2 receptor antagonist. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

Key facts

INN thiothixene hydrochloride
Brand THIOTHIXENE HYDROCHLORIDE
Mechanism Dopamine D2 receptor antagonist
Target D(2) dopamine receptor
Route INJECTION
Formulation INJECTABLE

Mechanism of action

Dopamine D2 receptor antagonist

Primary target: D(2) dopamine receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. aripiprazole Nervous system (N05)
  2. brexpiprazole Nervous system (N05)
  3. cabergoline Dopamine D2 receptor agonist
  4. clozapine Serotonin 2a (5-HT2a) receptor antagonist
  5. fluphenazine decanoate Dopamine D2 receptor antagonist
  6. fluphenazine hydrochloride Dopamine D2 receptor antagonist

Frequently asked questions

What is thiothixene hydrochloride?

thiothixene hydrochloride (THIOTHIXENE HYDROCHLORIDE) is a dopamine d2 receptor antagonist. Associated with Teva Pharma GmbH. Route of administration: injection. Current US regulatory status: approved.

What is the brand name for thiothixene hydrochloride?

THIOTHIXENE HYDROCHLORIDE is a marketed brand name for thiothixene hydrochloride. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of thiothixene hydrochloride?

thiothixene hydrochloride has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.