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Periciazine

Generic Name
Periciazine
Brand Names
Neuleptil
Drug Type
Small Molecule
Chemical Formula
C21H23N3OS
CAS Number
2622-26-6
Unique Ingredient Identifier
3405M6FD73

Overview

Periciazine is a phenothiazine of the piperidine group. It has been shown to reduce pathologic arousal and affective tension in some psychotic patients, while the symptoms of abnormal mental integration are relatively unaffected. It is a sedative phenothiazine with weak antipsychotic properties. It also has adrenolytic, anticholinergic, metabolic and endocrine effects and an action on the extrapyramidal system. It is used as an adjunctive medication in some psychotic patients, for the control of residual prevailing hostility, impulsiveness and aggressiveness. Pericyazine, like other phenothiazines, is presumed to act principally in the subcortical areas, by producing what has been described as a central adrenergic blockade.

Indication

For use as adjunctive medication in some psychotic patients. Propericiazine (Pericyazine)is used for the control of residual prevailing hostility, impulsiveness and aggressiveness.

Associated Conditions

  • Psychosis

Clinical Trials

Title
Posted
Study ID
Phase
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Sponsor

No clinical trials found

No clinical trials found for this drug

FDA Drug Approvals

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NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
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Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
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Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
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Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
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Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
Neulactil 2.5mg tablet blister pack
27524
Medicine
A
10/21/1991
Neulactil 10mg tablet blister pack
27523
Medicine
A
10/21/1991

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
NEULEPTIL
searchlight pharma inc
01926772
Capsule - Oral
10 MG
12/31/1969
NEULEPTIL
searchlight pharma inc
01926764
Capsule - Oral
20 MG
12/31/1976
NEULEPTIL
searchlight pharma inc
01926780
Capsule - Oral
5 MG
12/31/1969
NEULEPTIL
searchlight pharma inc
01926756
Drops - Oral
10 MG / ML
12/31/1976

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
NEMACTIL 50 mg COMPRIMIDOS RECUBIERTOS CON PELICULA
Sanofi Aventis S.A.
49193
COMPRIMIDO RECUBIERTO CON PELÍCULA
Medicamento Sujeto A Prescripción Médica
Not Commercialized
NEMACTIL 40mg/ml GOTAS ORALES EN SOLUCION
Neuraxpharm Spain S.L.
41573
GOTAS ORALES EN SOLUCIÓN
Medicamento Sujeto A Prescripción Médica
Commercialized
NEMACTIL 10 mg COMPRIMIDOS RECUBIERTOS CON PELICULA
Neuraxpharm Spain S.L.
42851
COMPRIMIDO RECUBIERTO CON PELÍCULA
Medicamento Sujeto A Prescripción Médica
Commercialized

Philippines FDA Drug Approvals

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License Number
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No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

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No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
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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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