Overview
A phenothiazine with actions similar to chlorpromazine. It is used as an antipsychotic and an antiemetic.
Indication
For the treatment of anxiety disorders, depressive symptoms secondary to anxiety and agitation.
Associated Conditions
- Agitation
- Psychosis
- Schizophrenia
- Acute non-psychotic Anxiety
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2019/05/29 | Phase 1 | Terminated | Adrianna Vlachos, MD | ||
2015/11/09 | N/A | Completed |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
|---|---|---|---|---|---|
| REMEDYREPACK INC. | 70518-2106 | ORAL | 5 mg in 1 1 | 2/27/2024 | |
| Mylan Pharmaceuticals Inc. | 0378-2410 | ORAL | 10 mg in 1 1 | 3/31/2015 | |
| State of Florida DOH Central Pharmacy | 53808-0629 | ORAL | 2 mg in 1 1 | 9/30/2013 | |
| Mylan Institutional Inc. | 51079-572 | ORAL | 1 mg in 1 1 | 12/16/2021 | |
| Mylan Institutional Inc. | 51079-574 | ORAL | 5 mg in 1 1 | 12/16/2021 | |
| Mylan Pharmaceuticals Inc. | 0378-2405 | ORAL | 5 mg in 1 1 | 3/31/2015 | |
| Mylan Pharmaceuticals Inc. | 0378-2401 | ORAL | 1 mg in 1 1 | 3/31/2015 | |
| Mylan Pharmaceuticals Inc. | 0378-2402 | ORAL | 2 mg in 1 1 | 3/31/2015 | |
| REMEDYREPACK INC. | 70518-2095 | ORAL | 2 mg in 1 1 | 2/27/2024 | |
| State of Florida DOH Central Pharmacy | 53808-0819 | ORAL | 10 mg in 1 1 | 9/30/2013 |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
|---|---|---|---|
| No EMA approvals found for this drug. | |||
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| AA PHARMA TRIFLUOPERAZINE TABLET 5 mg | SIN00289P | TABLET, FILM COATED | 5 mg | 4/21/1988 |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
|---|---|---|---|---|---|
| Trifluoperazine Hydrochloride Tablets | 国药准字H31021203 | 化学药品 | 片剂(糖衣) | 2/24/2020 | |
| Trifluoperazine Hydrochloride Tablets | 国药准字H44020394 | 化学药品 | 片剂 | 4/3/2020 |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
|---|---|---|---|---|---|
| No PPB approvals found for this drug. | |||||
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
|---|---|---|---|---|---|
| No TGA approvals found for this drug. | |||||
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