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    Prochlorperazine Dimaleate Salt

    ACTIVE PHARMA INGREDIENTS

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    01 2AJANTA PHARMA LTD

    02 2AMNEAL

    03 2BIONPHARMA

    04 2CEROVENE INC

    05 3CHARTWELL RX

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    01

    CHARTWELL RX

    U.S.A
    DIA 2025
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    CHARTWELL RX

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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : PROCHLORPERAZINE MALEATE

    Dosage Form : TABLET;ORAL

    Dosage Strength : EQ 5MG BASE

    Approval Date : 1996-07-19

    Application Number : 40101

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    GLAXOSMITHKLINE

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    RLD : Yes

    TE Code :

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    Dosage Strength : EQ 5MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 10571

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    03

    GLAXOSMITHKLINE

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    RLD : Yes

    TE Code :

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    Dosage Strength : EQ 10MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 10571

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    04

    GLAXOSMITHKLINE

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    RLD : Yes

    TE Code :

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    Dosage Strength : EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Approval Date : 1982-01-01

    Application Number : 10571

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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    05

    GLAXOSMITHKLINE

    United Kingdom
    DIA 2025
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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 1982-01-01

    Application Number : 11000

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    GLAXOSMITHKLINE

    United Kingdom
    DIA 2025
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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 15MG BASE

    Approval Date : 1982-01-01

    Application Number : 11000

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    GLAXOSMITHKLINE

    United Kingdom
    DIA 2025
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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 30MG BASE

    Approval Date : 1982-01-01

    Application Number : 11000

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    08

    GLAXOSMITHKLINE

    United Kingdom
    DIA 2025
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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 75MG BASE

    Approval Date : 1982-01-01

    Application Number : 11000

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    GLAXOSMITHKLINE

    United Kingdom
    DIA 2025
    Not Confirmed
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    DIA 2025
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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 10MG BASE

    Approval Date : 1999-10-06

    Application Number : 21019

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    10

    GLAXOSMITHKLINE

    United Kingdom
    DIA 2025
    Not Confirmed
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    GLAXOSMITHKLINE

    United Kingdom
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    DIA 2025
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    RLD : No

    TE Code :

    PROCHLORPERAZINE MALEATE

    Brand Name : COMPAZINE

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : EQ 15MG BASE

    Approval Date : 1999-10-06

    Application Number : 21019

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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