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    European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

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    Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.

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    Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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    TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

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

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    Lornoxicam

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    01 1GRUNENTHAL ITALIA Srl

    02 3Gr?nenthal Pharma Sa

    03 1Grindeks AS

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    Grindeks AS

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    Regulatory Info : Generic

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    Lornoxicam

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    Dosage Form : POWDER

    Dosage Strength : 8MG

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    Lornoxicam

    Brand Name : Noxon

    Dosage Form : Lornoxicam 8Mg 30 Joined' Oral Use

    Dosage Strength : 30 cpr riv 8 mg

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    Lornoxicam

    Brand Name : Taigalor

    Dosage Form : Lornoxicam 8Mg 30 Joined' Oral Use

    Dosage Strength : 30 cpr riv Div 8 mg

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    Regulatory Info : Deregistered

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    Lornoxicam

    Brand Name : Xefo

    Dosage Form : Film Coated Tablet

    Dosage Strength : 4mg

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    Approval Date : 12/04/1996

    Application Number : 19960412000013

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    Regulatory Info : Deregistered

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    Lornoxicam

    Brand Name : Xefo

    Dosage Form : Film Coated Tablet

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    Approval Date : 12/04/1996

    Application Number : 19960412000020

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    Regulatory Info : Deregistered

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    Lornoxicam

    Brand Name : Xefo

    Dosage Form : Solution For Injection

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    Approval Date : 23/01/1998

    Application Number : 19980123000027

    Regulatory Info : Deregistered

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    Regulatory Info : Deregistered

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    Lornoxicam

    Brand Name : Xefo Emergency

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    Approval Date : 07/03/2003

    Application Number : 20030307000049

    Regulatory Info : Deregistered

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    Regulatory Info : Cancelled

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    Lornoxicam

    Brand Name : Bosporon

    Dosage Form : Film Coated Tablet

    Dosage Strength : 8MG

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    Approval Date : 1999-07-01

    Application Number : 62691

    Regulatory Info : Cancelled

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    Turkey
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    Dosage Form : INJECTABLE, LYOPHILIZED POWDER

    Dosage Strength : 8MG

    Packaging : 1 Vial + 1 Solvent Or 3 Vials + 3 Solvents (Wfi)

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    Regulatory Info : Generic

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    Lornoxicam

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    Dosage Form : TABLET

    Dosage Strength : 4MG

    Packaging : 10 Or 20 Tablets

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    Regulatory Info : Generic

    Registration Country : Turkey

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