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    Polpharma is a Polish CDMO of APIs and a significant European API producer, delivering products to companies worldwide.

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    SPI Pharma has been solving formulation challenges using superior functional materials.

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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Suanfarma, at the Core of a Better Life.

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    Trifluoperazine Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    GLOBAL SALES INFORMATION

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    01 3AAIPharma Services Corp.

    02 4Actavis Inc

    03 4Athem Pharma

    04 1Chartwell Pharmaceuticals llc

    05 4DURAMED PHARMS BARR

    06 6GSK

    07 4IVAX Pharmaceuticals Inc

    08 2Lucent Biotech Ltd

    09 1Quad Pharma

    10 6RELIANCE FORMULATION PVT. LTD

    11 4Sandoz B2B

    12 4Viatris

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    01

    Actavis Inc

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1988-06-23

    Application Number : 85973

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

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    Approval Date : 1988-06-23

    Application Number : 85975

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

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    Approval Date : 1988-06-23

    Application Number : 85976

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 1988-06-23

    Application Number : 88710

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    Athem Pharma

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

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    Approval Date : 1996-10-25

    Application Number : 40153

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    Registration Country : USA

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    Athem Pharma

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

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    Approval Date : 1996-10-25

    Application Number : 40153

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    Registration Country : USA

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    Athem Pharma

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    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1996-10-25

    Application Number : 40153

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    Registration Country : USA

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    Athem Pharma

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1996-10-25

    Application Number : 40153

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Chartwell Pharmaceuticals llc

    U.S.A
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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1982-04-15

    Application Number : 85787

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    DURAMED PHARMS BARR

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    DURAMED PHARMS BARR

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 1985-04-23

    Application Number : 88967

    Regulatory Info : DISCN

    Registration Country : USA

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    DURAMED PHARMS BARR

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 1985-04-23

    Application Number : 88968

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    GSK

    United Kingdom
    Pharma Live Expo
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    GSK

    United Kingdom
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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : STELAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    GSK

    United Kingdom
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    GSK

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    Regulatory Info : DISCN

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : STELAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    GSK

    United Kingdom
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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : STELAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    GSK

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : STELAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    GSK

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : STELAZINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 2MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    GSK

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : STELAZINE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    IVAX Pharmaceuticals Inc

    U.S.A
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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1982-11-19

    Application Number : 87328

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    IVAX Pharmaceuticals Inc

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 1982-11-19

    Application Number : 87612

    Regulatory Info : DISCN

    Registration Country : USA

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    IVAX Pharmaceuticals Inc

    U.S.A
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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 1982-11-19

    Application Number : 87613

    Regulatory Info : DISCN

    Registration Country : USA

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    IVAX Pharmaceuticals Inc

    U.S.A
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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1982-11-19

    Application Number : 87614

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Sandoz B2B

    Switzerland
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    Switzerland
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    Regulatory Info : RX

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85785

    Regulatory Info : RX

    Registration Country : USA

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    23

    Sandoz B2B

    Switzerland
    Pharma Live Expo
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    Sandoz B2B

    Switzerland
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    Regulatory Info : RX

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85786

    Regulatory Info : RX

    Registration Country : USA

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    24

    Sandoz B2B

    Switzerland
    Pharma Live Expo
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
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    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85788

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    25

    Sandoz B2B

    Switzerland
    Pharma Live Expo
    Not Confirmed
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    Sandoz B2B

    Switzerland
    arrow
    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag Switzerland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85789

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

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    26

    Viatris

    U.S.A
    Pharma Live Expo
    Not Confirmed
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    Viatris

    U.S.A
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    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 1997-07-07

    Application Number : 40209

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    27

    Viatris

    U.S.A
    Pharma Live Expo
    Not Confirmed
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    Viatris

    U.S.A
    arrow
    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 2MG BASE

    Packaging :

    Approval Date : 1997-07-07

    Application Number : 40209

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    28

    Viatris

    U.S.A
    Pharma Live Expo
    Not Confirmed
    arrow

    Viatris

    U.S.A
    arrow
    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1997-07-07

    Application Number : 40209

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    29

    Viatris

    U.S.A
    Pharma Live Expo
    Not Confirmed
    arrow

    Viatris

    U.S.A
    arrow
    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : RX

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1997-07-07

    Application Number : 40209

    Regulatory Info : RX

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

    Digital Content

    Website

    Corporate PDF

    30

    Wockhardt

    India
    Pharma Live Expo
    Not Confirmed
    arrow

    Wockhardt

    India
    arrow
    Pharma Live Expo
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    Regulatory Info : DISCN

    Registration Country : USA

    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1983-07-26

    Application Number : 88143

    Regulatory Info : DISCN

    Registration Country : USA

    blank

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    Product Web Link

    Virtual Booth

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    Website

    Corporate PDF