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    Egis is a Hungarian generic pharma company with 110 years history. Our activities incorporate all areas of the pharma value chain.

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    Kewpie is your partner for Sodium Hyaluronate & Hyaluronic Acid// CEP, USDMF, KDMF & JDMF registered.

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    Centrient is a leading manufacturer of Beta-Lactam Antibiotics and a provider of next-generation Statins and Antifungals.

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    AbbVie CDMO has been working with global companies to develop, manufacture & scale biopharmaceutical products.

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    IMIPRAMINE HCL

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    Sanofi

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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : PRESAMINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG

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    Approval Date : 1982-01-01

    Application Number : 11836

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    Imipramine hydrochloride

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    Strides Pharma Science

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    Approval Date : 1983-10-21

    Application Number : 88262

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    04

    Sanofi

    France
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    05

    Sanofi

    France
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    IMIPRAMINE HYDROCHLORIDE

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    Approval Date : 1982-01-01

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    Aspen Pharmacare Holdings

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    Imipramine hydrochloride

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    Aspen Pharmacare Holdings

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    Aspen Pharmacare Holdings

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    09

    Strides Pharma Science

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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

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    Approval Date : 1983-10-21

    Application Number : 88276

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    10

    Strides Pharma Science

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    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1983-10-21

    Application Number : 88292

    Regulatory Info : RX

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    11

    Strides Pharma Science

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    12

    Strides Pharma Science

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    Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

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    13

    Strides Pharma Science

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    Imipramine Hydrochloride

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    Dosage Form : Tablet

    Dosage Strength : 50MG

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    14

    Abbott Laboratories

    U.S.A
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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : JANIMINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 1982-01-01

    Application Number : 17895

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    Registration Country : USA

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    15

    Abbott Laboratories

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    Brand Name : JANIMINE

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    Approval Date : 1982-01-01

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    16

    Abbott Laboratories

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    Approval Date : 1982-01-01

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    17

    Leading Pharma, LLC

    U.S.A
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    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2012-10-24

    Application Number : 40903

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    Leading Pharma, LLC

    U.S.A
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    Brand Name : IMIPRAMINE HYDROCHLORIDE

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    Approval Date : 2012-10-24

    Application Number : 40903

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    Leading Pharma, LLC

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    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

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    Approval Date : 2012-10-24

    Application Number : 40903

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    Novartis Pharmaceuticals Corporatio...

    Switzerland
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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : TOFRANIL

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 12.5MG/ML

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    Approval Date : 1982-01-01

    Application Number : 11838

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    Oxford Pharm

    U.S.A
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    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

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    Approval Date : 2008-02-28

    Application Number : 40751

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    Registration Country : USA

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    22

    Oxford Pharm

    U.S.A
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    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG

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    Approval Date : 2008-02-28

    Application Number : 40751

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    Oxford Pharm

    U.S.A
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    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2008-02-28

    Application Number : 40751

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    Sandoz B2B

    Switzerland
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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83745

    Regulatory Info : RX

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    Sun Pharmaceutical Industries Limit...

    India
    Peptide Therapy Summit
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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 1990-06-05

    Application Number : 81048

    Regulatory Info : DISCN

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    Sun Pharmaceutical Industries Limit...

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    Regulatory Info : RX

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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG

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    Approval Date : 1990-06-05

    Application Number : 81049

    Regulatory Info : RX

    Registration Country : USA

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    Sun Pharmaceutical Industries Limit...

    India
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    Sun Pharmaceutical Industries Limit...

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    Regulatory Info : RX

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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 1990-06-05

    Application Number : 81050

    Regulatory Info : RX

    Registration Country : USA

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    Teva Pharmaceutical Industries

    Israel
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    Regulatory Info : DISCN

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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83729

    Regulatory Info : DISCN

    Registration Country : USA

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    29

    Teva Pharmaceutical Industries

    Israel
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    Teva Pharmaceutical Industries

    Israel
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    Regulatory Info : DISCN

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    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 50MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83729

    Regulatory Info : DISCN

    Registration Country : USA

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    30

    Teva Pharmaceutical Industries

    Israel
    Peptide Therapy Summit
    Not Confirmed
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    Teva Pharmaceutical Industries

    Israel
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    Peptide Therapy Summit
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    IMIPRAMINE HYDROCHLORIDE

    Brand Name : IMIPRAMINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 25MG

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 83729

    Regulatory Info : DISCN

    Registration Country : USA

    blank

    Portfolio PDF

    Product Web Link

    Virtual Booth

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    Website

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