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    Actavis Inc

    Ireland
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

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    DICLOFENAC SODIUM; MISOPROSTOL

    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

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    Amneal Pharmaceuticals

    U.S.A
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 50MG;0.2MG

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    Approval Date : 2016-11-25

    Application Number : 203995

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    DICLOFENAC SODIUM; MISOPROSTOL

    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 75MG;0.2MG

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    Approval Date : 2016-11-25

    Application Number : 203995

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    ANI Pharmaceuticals Inc

    U.S.A
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    Approval Date : 2002-07-10

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    ANI Pharmaceuticals Inc

    U.S.A
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    Exela Pharma Sciences, LLC.

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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 50MG;0.2MG

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    Approval Date : 2014-03-14

    Application Number : 200540

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    Registration Country : USA

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    Exela Pharma Sciences, LLC.

    U.S.A
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 75MG;0.2MG

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    Approval Date : 2014-03-14

    Application Number : 200540

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    09

    Micro Labs Limited

    India
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 50MG;0.2MG

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    Approval Date : 2021-07-15

    Application Number : 204355

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    Registration Country : USA

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    10

    Micro Labs Limited

    India
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    India
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    DICLOFENAC SODIUM; MISOPROSTOL

    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 75MG;0.2MG

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    Approval Date : 2021-07-15

    Application Number : 204355

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    Registration Country : USA

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    11

    Novel Laboratories, Inc.

    U.S.A
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    MISOPROSTOL

    Brand Name : MISOPROSTOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.1MG

    Packaging :

    Approval Date : 2012-07-25

    Application Number : 91667

    Regulatory Info : DISCN

    Registration Country : USA

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    12

    Novel Laboratories, Inc.

    U.S.A
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    MISOPROSTOL

    Brand Name : MISOPROSTOL

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.2MG

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    Approval Date : 2012-07-25

    Application Number : 91667

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    Registration Country : USA

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    13

    Pfizer Inc

    U.S.A
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    MISOPROSTOL

    Brand Name : CYTOTEC

    Dosage Form : TABLET;ORAL

    Dosage Strength : 0.2MG

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    Approval Date : 1988-12-27

    Application Number : 19268

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    Registration Country : USA

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    Pfizer Inc

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    Brand Name : CYTOTEC

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    Approval Date : 1990-09-21

    Application Number : 19268

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    Registration Country : USA

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    Brand Name : ARTHROTEC

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 50MG;0.2MG

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    Approval Date : 1997-12-24

    Application Number : 20607

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    Registration Country : USA

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    Pfizer Inc

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    Brand Name : ARTHROTEC

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    Dosage Strength : 75MG;0.2MG

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    Approval Date : 1997-12-24

    Application Number : 20607

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    Sandoz B2B

    Switzerland
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 50MG;0.2MG

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    Approval Date : 2013-05-09

    Application Number : 200158

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    Registration Country : USA

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    Sandoz B2B

    Switzerland
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 75MG;0.2MG

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    Approval Date : 2013-05-09

    Application Number : 200158

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    Yung Shin Pharmaceutical Industrial

    China
    American Pharma Summit
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    China
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 50MG;0.2MG

    Packaging :

    Approval Date : 2020-02-19

    Application Number : 205143

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    Registration Country : USA

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    Yung Shin Pharmaceutical Industrial

    China
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    Brand Name : DICLOFENAC SODIUM AND MISOPROSTOL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 75MG;0.2MG

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    Approval Date : 2020-02-19

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