Overview
An antipsychotic phenothiazine derivative with actions and uses similar to those of chlorpromazine.
Indication
For use in the management of the manifestations of psychotic disorders and for the control of severe nausea and vomiting in adults.
Associated Conditions
- Anxiety
- Depression
- Schizophrenia
- Moderate Agitation
- Moderate Anxiety
- Moderate Depressed mood
- Severe Anxiety
- Severe Depressed mood
- Severe Nausea and vomiting
- Severe agitation
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2023/03/09 | Phase 2 | Recruiting | |||
2021/03/01 | Phase 1 | Completed | |||
2020/10/28 | Phase 3 | Recruiting | Jennifer Holder-Murray | ||
2016/09/08 | N/A | Terminated | |||
2015/11/09 | N/A | Completed | |||
2015/05/01 | Phase 3 | Completed | |||
2015/03/02 | Phase 3 | Terminated | |||
2014/12/04 | Phase 4 | Completed | Technical University of Munich | ||
2014/07/24 | Phase 4 | Completed | |||
2010/09/01 | Phase 4 | Withdrawn |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
State of Florida DOH Central Pharmacy | 53808-0665 | ORAL | 4 mg in 1 1 | 8/18/2010 | |
Mylan Pharmaceuticals Inc. | 0378-0042 | ORAL | 4 mg in 1 1 | 9/26/2019 | |
Actavis Pharma, Inc. | 0591-4103 | ORAL | 8 mg in 1 1 | 5/31/2017 | |
Proficient Rx LP | 71205-843 | ORAL | 8 mg in 1 1 | 2/1/2023 | |
Bryant Ranch Prepack | 72162-1163 | ORAL | 4 mg in 1 1 | 9/16/2022 | |
State of Florida DOH Central Pharmacy | 53808-0762 | ORAL | 16 mg in 1 1 | 8/18/2010 | |
Zydus Pharmaceuticals (USA) Inc. | 68382-594 | ORAL | 16 mg in 1 1 | 9/30/2023 | |
Major Pharmaceuticals | 0904-6601 | ORAL | 8 mg in 1 1 | 12/18/2018 | |
Mylan Pharmaceuticals Inc. | 0378-0442 | ORAL | 2 mg in 1 1 | 9/26/2019 | |
Bryant Ranch Prepack | 63629-2251 | ORAL | 4 mg in 1 1 | 4/6/2021 |
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 |
---|---|---|---|---|---|
APO-PERPHENAZINE TABLET 8 mg | SIN00437P | TABLET, FILM COATED | 8 mg | 4/27/1988 | |
APO-PERPHENAZINE TABLET 4 mg | SIN00444P | TABLET, FILM COATED | 4 mg | 4/27/1988 |
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 |
---|---|---|---|---|---|
PERPHENAZINE | aa pharma inc | 00335118 | Tablet - Oral | 8 MG | 12/31/1976 |
PHENAZINE 4 TAB | icn canada ltd. | 00296317 | Tablet - Oral | 4 MG / TAB | 12/31/1973 |
PERPHENAZINE TAB 4MG | PRO DOC LIMITEE | 00563749 | Tablet - Oral | 4 MG | 12/31/1982 |
PERPHENAZINE 2 TAB 2MG | PRO DOC LIMITEE | 00563757 | Tablet - Oral | 2 MG | 12/31/1982 |
PMS PERPHENAZINE TAB 8MG | 00726281 | Tablet - Oral | 8 MG | 12/31/1987 | |
PMS PERPHENAZINE TAB 4MG | 00726192 | Tablet - Oral | 4 MG | 12/31/1987 | |
PERPHENAZINE | aa pharma inc | 00335134 | Tablet - Oral | 2 MG | 12/31/1976 |
PERPHENAZINE 16 TAB | PRO DOC LIMITEE | 00563722 | Tablet - Oral | 16 MG | 12/31/1982 |
PERPHENAZINE | aa pharma inc | 00335096 | Tablet - Oral | 16 MG | 12/31/1976 |
PERPHENAZINE TAB 4MG | d.c. labs limited | 00456047 | Tablet - Oral | 4 MG | 12/31/1979 |
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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