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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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    Prochlorperazine Maleate

    ACTIVE PHARMA INGREDIENTS

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    01 2AAIPharma Services Corp.

    02 3Actavis Inc

    03 1Adcock Ingram

    04 2Ajanta Pharma Limited

    05 2Amneal Pharmaceuticals

    06 2Bionpharma

    07 3Chartwell Pharmaceuticals llc

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    01

    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 1982-01-01

    Application Number : 85178

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Actavis Inc

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 1982-01-01

    Application Number : 85579

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Actavis Inc

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1982-01-01

    Application Number : 85580

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    Chartwell Pharmaceuticals llc

    U.S.A
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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1996-07-19

    Application Number : 40101

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    Chartwell Pharmaceuticals llc

    U.S.A
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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 1996-07-19

    Application Number : 40101

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Chartwell Pharmaceuticals llc

    U.S.A
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    Chartwell Pharmaceuticals llc

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

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    Approval Date : 1996-07-19

    Application Number : 40101

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    DURAMED PHARMS BARR

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1997-05-01

    Application Number : 40207

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    DURAMED PHARMS BARR

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1997-05-01

    Application Number : 40207

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    DURAMED PHARMS BARR

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1987-01-20

    Application Number : 89484

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    DURAMED PHARMS BARR

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    ELCC
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    ELCC
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1987-01-20

    Application Number : 89485

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    DURAMED PHARMS BARR

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    ELCC
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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 25MG BASE

    Packaging :

    Approval Date : 1987-01-20

    Application Number : 89486

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    Not Confirmed
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    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 : 10571

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    GSK

    United Kingdom
    ELCC
    Not Confirmed
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    GSK

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    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 : 10571

    Regulatory Info : DISCN

    Registration Country : USA

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    14

    GSK

    United Kingdom
    ELCC
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    GSK

    United Kingdom
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    ELCC
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    Regulatory Info : DISCN

    Registration Country : USA

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : TABLET;ORAL

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

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 10571

    Regulatory Info : DISCN

    Registration Country : USA

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    15

    GSK

    United Kingdom
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    Regulatory Info : DISCN

    Registration Country : USA

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11000

    Regulatory Info : DISCN

    Registration Country : USA

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    16

    GSK

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    Regulatory Info : DISCN

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    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 15MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11000

    Regulatory Info : DISCN

    Registration Country : USA

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    17

    GSK

    United Kingdom
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    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 30MG BASE

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    Approval Date : 1982-01-01

    Application Number : 11000

    Regulatory Info : DISCN

    Registration Country : USA

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    18

    GSK

    United Kingdom
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    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 75MG BASE

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11000

    Regulatory Info : DISCN

    Registration Country : USA

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    19

    GSK

    United Kingdom
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    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1999-10-06

    Application Number : 21019

    Regulatory Info : DISCN

    Registration Country : USA

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    20

    GSK

    United Kingdom
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    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 15MG BASE

    Packaging :

    Approval Date : 1999-10-06

    Application Number : 21019

    Regulatory Info : DISCN

    Registration Country : USA

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    21

    IVAX Pharmaceuticals Inc

    U.S.A
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    IVAX Pharmaceuticals Inc

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1998-01-20

    Application Number : 40162

    Regulatory Info : DISCN

    Registration Country : USA

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    IVAX Pharmaceuticals Inc

    U.S.A
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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

    Packaging :

    Approval Date : 1998-01-20

    Application Number : 40162

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    Registration Country : USA

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    Jubilant Cadista Pharmaceuticals

    U.S.A
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    Jubilant Cadista Pharmaceuticals

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCOMP

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Packaging :

    Approval Date : 1998-02-27

    Application Number : 40268

    Regulatory Info : RX

    Registration Country : USA

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    Jubilant Cadista Pharmaceuticals

    U.S.A
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    Jubilant Cadista Pharmaceuticals

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCOMP

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    Approval Date : 1998-02-27

    Application Number : 40268

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    Approval Date : 2022-06-13

    Application Number : 216202

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    Novitium Pharma LLC

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    Approval Date : 2022-06-13

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    Teva Pharmaceutical Industries

    Israel
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    Brand Name : PROCHLORPERAZINE MALEATE

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    Approval Date : 1996-07-11

    Application Number : 40120

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    Teva Pharmaceutical Industries

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

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    Dosage Strength : EQ 10MG BASE

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    Approval Date : 1996-07-11

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    NORVIUM BIOSCIENCE

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    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 10MG BASE

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    Approval Date : 1996-10-28

    Application Number : 40185

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    NORVIUM BIOSCIENCE

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    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

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    Approval Date : 1996-10-28

    Application Number : 40185

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