MedPath

Perphenazine

Generic Name
Perphenazine
Drug Type
Small Molecule
Chemical Formula
C21H26ClN3OS
CAS Number
58-39-9
Unique Ingredient Identifier
FTA7XXY4EZ

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Withdrawn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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