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    DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

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    Valsynthese, part of the SSE Group, is a CDMO focused on highly energetic and highly hazardous chemistry.

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    xyz-pharma-m-2024-10-07

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    With Fermion, start the journey of your innovative API.

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    Bloomage is a one-stop source for CEP Sodium Hyaluronate and Hyaluronic Acid// FDA-inspected & GMP-certified.

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    xyz-pharma-m-2024-10-07

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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

    13 1Wockhardt

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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

    Regulatory Info : DISCN

    Registration Country : USA

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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

    Regulatory Info : DISCN

    Registration Country : USA

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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

    U.S.A
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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

    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 : 1996-10-25

    Application Number : 40153

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Athem Pharma

    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 : 1996-10-25

    Application Number : 40153

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Athem Pharma

    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 : 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
    Antibody Engineering
    Not Confirmed
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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

    United Kingdom
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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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    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**

    Packaging :

    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

    United Kingdom
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    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    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 : 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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    Regulatory Info : DISCN

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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

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    Regulatory Info : DISCN

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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
    Antibody Engineering
    Not Confirmed
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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 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
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    Sandoz B2B

    Switzerland
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    Antibody Engineering
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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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    Sandoz B2B

    Switzerland
    Antibody Engineering
    Not Confirmed
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    Sandoz B2B

    Switzerland
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    Antibody Engineering
    Not Confirmed
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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
    Antibody Engineering
    Not Confirmed
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    Switzerland
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    Antibody Engineering
    Not Confirmed
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    Regulatory Info : RX

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    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
    Antibody Engineering
    Not Confirmed
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    Viatris

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    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
    Antibody Engineering
    Not Confirmed
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    Viatris

    U.S.A
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    Antibody Engineering
    Not Confirmed
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    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
    Antibody Engineering
    Not Confirmed
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    Viatris

    U.S.A
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
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    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
    Antibody Engineering
    Not Confirmed
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    Viatris

    U.S.A
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    Antibody Engineering
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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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 : 1997-07-07

    Application Number : 40209

    Regulatory Info : RX

    Registration Country : USA

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    30

    Wockhardt

    India
    Antibody Engineering
    Not Confirmed
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    Wockhardt

    India
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    Antibody Engineering
    Not Confirmed
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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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