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    01

    Actavis Inc

    Ireland
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 10MG BASE/ML

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    Approval Date : 1982-06-08

    Application Number : 87153

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    02

    Actavis Inc

    Ireland
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : SYRUP;ORAL

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    Approval Date : 1982-09-01

    Application Number : 87154

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    03

    Actavis Inc

    Ireland
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1987-07-08

    Application Number : 89530

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    04

    Actavis Inc

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1987-07-08

    Application Number : 89605

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    05

    Actavis Inc

    Ireland
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

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    Approval Date : 1987-07-08

    Application Number : 89606

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    06

    Baxter Healthcare Corporation

    U.S.A
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1982-10-01

    Application Number : 87759

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    07

    GSK

    United Kingdom
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : COMPAZINE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG 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 : 10742

    Regulatory Info : DISCN

    Registration Country : USA

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    GSK

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    Regulatory Info : DISCN

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : COMPAZINE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : EQ 5MG BASE/5ML

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    Approval Date : 1982-01-01

    Application Number : 11188

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    09

    GSK

    United Kingdom
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    GSK

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : COMPAZINE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 10MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11276

    Regulatory Info : DISCN

    Registration Country : USA

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    10

    Hikma Pharmaceuticals

    United Kingdom
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1988-05-03

    Application Number : 89523

    Regulatory Info : DISCN

    Registration Country : USA

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    11

    Hospira, Inc.

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1988-04-07

    Application Number : 89703

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Morton Grove Pharmaceuticals

    U.S.A
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    Morton Grove Pharmaceuticals

    U.S.A
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : EQ 5MG BASE/5ML

    Packaging :

    Approval Date : 1984-10-25

    Application Number : 88597

    Regulatory Info : DISCN

    Registration Country : USA

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    13

    Morton Grove Pharmaceuticals

    U.S.A
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : CONCENTRATE;ORAL

    Dosage Strength : EQ 10MG BASE/ML

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    Approval Date : 1984-10-25

    Application Number : 88598

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    Registration Country : USA

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    14

    Quad Pharma

    South Africa
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    Dosage Form : Injectable; Injection

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    Application Number : 89637

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    Quad Pharma

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    Application Number : 89638

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    Sagent Pharmaceuticals

    U.S.A
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    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2004-05-28

    Application Number : 40540

    Regulatory Info : RX

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    17

    SMITH & NEPHEW INC

    Canada
    STLE Annual Meeting
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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 1986-12-04

    Application Number : 89251

    Regulatory Info : DISCN

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    18

    Teva Pharmaceutical Industries

    Israel
    STLE Annual Meeting
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    Israel
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    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

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    Approval Date : 2003-05-30

    Application Number : 40505

    Regulatory Info : DISCN

    Registration Country : USA

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    Wyeth Pharmaceuticals Inc

    U.S.A
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86348

    Regulatory Info : DISCN

    Registration Country : USA

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    MARSAM PHARMS LLC

    Country
    STLE Annual Meeting
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    Regulatory Info : DISCN

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    PROCHLORPERAZINE EDISYLATE

    Brand Name : PROCHLORPERAZINE EDISYLATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : EQ 5MG BASE/ML

    Packaging :

    Approval Date : 1988-12-05

    Application Number : 89675

    Regulatory Info : DISCN

    Registration Country : USA

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