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    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Fluphenazine

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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

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    FAMAR CDMO- From early development to commercial manufacturing.

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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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    01 4Dr. Reddy's Laboratories

    02 4Breckenridge Pharmaceutical

    03 3AAIPharma Services Corp.

    04 2ANI Pharmaceuticals Inc

    05 4Actavis Inc

    06 4Ajanta Pharma Limited

    07 4Alembic Pharmaceuticals Limited

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    25 5Sandoz B2B

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    Dr. Reddy's Laboratories

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

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    Approval Date : 2021-01-07

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    Breckenridge Pharmaceutical

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

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    Dosage Strength : 1MG

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    Approval Date : 2022-11-15

    Application Number : 216891

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    Dr. Reddy's Laboratories

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2021-01-07

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    Dr. Reddy's Laboratories

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2021-01-07

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    Dr. Reddy's Laboratories

    India
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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2021-01-07

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    Breckenridge Pharmaceutical

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    Brand Name : FLUPHENAZINE HYDROCHLORIDE

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    Dosage Strength : 2.5MG

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    Approval Date : 2022-11-15

    Application Number : 216891

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    07

    Breckenridge Pharmaceutical

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2022-11-15

    Application Number : 216891

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    Breckenridge Pharmaceutical

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    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2022-11-15

    Application Number : 216891

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    09

    Actavis Inc

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    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 1987-12-18

    Application Number : 88527

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    Actavis Inc

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG

    Packaging :

    Approval Date : 1987-12-18

    Application Number : 88544

    Regulatory Info : DISCN

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    11

    Actavis Inc

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1987-12-18

    Application Number : 88550

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    12

    Actavis Inc

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 1MG

    Packaging :

    Approval Date : 1987-12-18

    Application Number : 88555

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    ANI Pharmaceuticals Inc

    U.S.A
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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : 5MG/ML

    Packaging :

    Approval Date : 1991-08-30

    Application Number : 73058

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    ANI Pharmaceuticals Inc

    U.S.A
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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : ELIXIR;ORAL

    Dosage Strength : 2.5MG/5ML

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    Approval Date : 1993-04-29

    Application Number : 81310

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    15

    Bayer AG

    Germany
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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PERMITIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.25MG

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    Approval Date : 1982-01-01

    Application Number : 12034

    Regulatory Info : DISCN

    Registration Country : USA

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    Bayer AG

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    Brand Name : PERMITIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG

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    Approval Date : 1982-01-01

    Application Number : 12034

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    17

    Bayer AG

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    Brand Name : PERMITIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 1982-01-01

    Application Number : 12034

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    18

    Bayer AG

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PERMITIL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1982-01-01

    Application Number : 12034

    Regulatory Info : DISCN

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    19

    Bayer AG

    Germany
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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PERMITIL

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 1MG

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    Approval Date : 1982-01-01

    Application Number : 12419

    Regulatory Info : DISCN

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    Bayer AG

    Germany
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    Bayer AG

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PERMITIL

    Dosage Form : CONCENTRATE;ORAL

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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 16008

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    Bristol Myers Squibb

    U.S.A
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    Not Confirmed
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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : TABLET;ORAL

    Dosage Strength : 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11751

    Regulatory Info : DISCN

    Registration Country : USA

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    22

    Bristol Myers Squibb

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    Regulatory Info : DISCN

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11751

    Regulatory Info : DISCN

    Registration Country : USA

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    23

    Bristol Myers Squibb

    U.S.A
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    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    Regulatory Info : DISCN

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11751

    Regulatory Info : DISCN

    Registration Country : USA

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    Bristol Myers Squibb

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    Bristol Myers Squibb

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    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11751

    Regulatory Info : DISCN

    Registration Country : USA

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    25

    Bristol Myers Squibb

    U.S.A
    BioAsia
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioAsia
    Not Confirmed
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    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 2.5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11751

    Regulatory Info : DISCN

    Registration Country : USA

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    26

    Bristol Myers Squibb

    U.S.A
    BioAsia
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : ELIXIR;ORAL

    Dosage Strength : 2.5MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12145

    Regulatory Info : DISCN

    Registration Country : USA

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    27

    Bristol Myers Squibb

    U.S.A
    BioAsia
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    FLUPHENAZINE ENANTHATE

    Brand Name : PROLIXIN ENANTHATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 16110

    Regulatory Info : DISCN

    Registration Country : USA

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    28

    Bristol Myers Squibb

    U.S.A
    BioAsia
    Not Confirmed
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    Bristol Myers Squibb

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : PROLIXIN

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : 5MG/ML

    Packaging :

    Approval Date : 1985-11-07

    Application Number : 70533

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    PHARM ASSOC

    U.S.A
    BioAsia
    Not Confirmed
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    PHARM ASSOC

    U.S.A
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    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : ELIXIR;ORAL

    Dosage Strength : 2.5MG/5ML

    Packaging :

    Approval Date : 1996-08-21

    Application Number : 40146

    Regulatory Info : RX

    Registration Country : USA

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    30

    PHARM ASSOC

    U.S.A
    BioAsia
    Not Confirmed
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    PHARM ASSOC

    U.S.A
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    BioAsia
    Not Confirmed
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    Regulatory Info : RX

    Registration Country : USA

    FLUPHENAZINE HYDROCHLORIDE

    Brand Name : FLUPHENAZINE HYDROCHLORIDE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : 5MG/ML

    Packaging :

    Approval Date : 1996-09-16

    Application Number : 74725

    Regulatory Info : RX

    Registration Country : USA

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