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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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    Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.

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    Trifluoperazine Hydrochloride

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

    EXCIPIENTS BY APPLICATIONS

    GLOBAL SALES INFORMATION

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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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

    Ireland
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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

    Regulatory Info : DISCN

    Registration Country : USA

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    Actavis Inc

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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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    03

    Actavis Inc

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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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    04

    Actavis Inc

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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

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Athem Pharma

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    TRIFLUOPERAZINE HYDROCHLORIDE

    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 1MG BASE

    Packaging :

    Approval Date : 1996-10-25

    Application Number : 40153

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    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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    07

    Athem Pharma

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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 : 1996-10-25

    Application Number : 40153

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    Registration Country : USA

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    08

    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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    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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    11

    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
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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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    GSK

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    Regulatory Info : DISCN

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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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    Regulatory Info : DISCN

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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

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    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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    IVAX Pharmaceuticals Inc

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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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    20

    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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    21

    IVAX Pharmaceuticals Inc

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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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    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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    Sandoz B2B

    Switzerland
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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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    Sandoz B2B

    Switzerland
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    Sandoz B2B

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    ELCC
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    Flag Switzerland
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    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

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    Sandoz B2B

    Switzerland
    ELCC
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    ELCC
    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
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    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

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    26

    Viatris

    U.S.A
    ELCC
    Not Confirmed
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    Viatris

    U.S.A
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    ELCC
    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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    Flag U.S.A
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    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

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    27

    Viatris

    U.S.A
    ELCC
    Not Confirmed
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    Viatris

    U.S.A
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    ELCC
    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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    Flag U.S.A
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    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

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    28

    Viatris

    U.S.A
    ELCC
    Not Confirmed
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    Viatris

    U.S.A
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    ELCC
    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

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    29

    Viatris

    U.S.A
    ELCC
    Not Confirmed
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    Viatris

    U.S.A
    arrow
    ELCC
    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 10MG BASE

    Packaging :

    Approval Date : 1997-07-07

    Application Number : 40209

    Regulatory Info : RX

    Registration Country : USA

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    30

    Wockhardt

    India
    ELCC
    Not Confirmed
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    Wockhardt

    India
    arrow
    ELCC
    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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    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

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