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    With Fermion, start the journey of your innovative API.

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    Suanfarma CDMO offers integrated end-to-end solutions for development & commercialization of intermediates & APIs for small molecules.

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    01 4Actavis Inc

    02 4Athem Pharma

    03 1Chartwell Pharmaceuticals llc

    04 4DURAMED PHARMS BARR

    05 6GSK

    06 4IVAX Pharmaceuticals Inc

    07 2Lucent Biotech Ltd

    08 1Quad Pharma

    09 6RELIANCE FORMULATION PVT. LTD

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    01

    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

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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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    02

    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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    03

    Athem Pharma

    U.S.A
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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

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Athem Pharma

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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

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    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 10MG BASE

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    Approval Date : 1996-10-25

    Application Number : 40153

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    Registration Country : USA

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    06

    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

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    Approval Date : 1982-04-15

    Application Number : 85787

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    Registration Country : USA

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    07

    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**

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    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    GSK

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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**

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    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    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**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11552

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    GSK

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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 10MG 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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    11

    GSK

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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**

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    Approval Date : 1982-01-01

    Application Number : 11552

    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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    Regulatory Info : DISCN

    Registration Country : USA

    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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    13

    Sandoz B2B

    Switzerland
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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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    14

    Sandoz B2B

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    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

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    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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    16

    Sandoz B2B

    Switzerland
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    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1982-01-01

    Application Number : 85789

    Regulatory Info : RX

    Registration Country : USA

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    17

    Viatris

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    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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    Viatris

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    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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    19

    Viatris

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    Brand Name : TRIFLUOPERAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1997-07-07

    Application Number : 40209

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    Registration Country : USA

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    Viatris

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    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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