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 |
|---|---|---|---|---|---|
| No NMPA approvals found for this drug. | |||||
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. | |||||
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
|---|---|---|---|---|---|
| NOVO-TRIFLUZINE - TAB 5MG | novopharm limited | 00021873 | Tablet - Oral | 5.9 MG | 12/31/1971 |
| NOVO-TRIFLUZINE - TAB 10MG | novopharm limited | 00021881 | Tablet - Oral | 11.8 MG | 12/31/1971 |
| PMS TRIFLUOPERAZINE TAB 20MG | 00726257 | Tablet - Oral | 20 MG / TAB | 12/31/1988 | |
| PMS TRIFLUOPERAZINE TAB 1MG | 00726214 | Tablet - Oral | 1 MG / TAB | 12/31/1988 | |
| NOVO-TRIFLUZINE - TAB 2MG | novopharm limited | 00021865 | Tablet - Oral | 2.36 MG | 12/31/1971 |
| NOVO-FLURAZINE TAB 20MG | novopharm limited | 00255149 | Tablet - Oral | 23.6 MG / TAB | 12/31/1971 |
| NOVO-FLURAZINE TAB 1MG | novopharm limited | 00021857 | Tablet - Oral | 1.18 MG / TAB | 12/31/1971 |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
|---|---|---|---|---|---|
| No CIMA AEMPS (Spain) approvals found for this drug. | |||||
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Philippines FDA approvals found for this drug. | |||||
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Saudi SFDA approvals found for this drug. | |||||
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
|---|---|---|---|---|---|
| No Malaysia NPRA approvals found for this drug. | |||||
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
|---|---|---|---|---|---|
| No UK EMC drug information found for this drug. | |||||
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