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    Moclobemide

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    14 5Paranova Pharmaceuticals Ab

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    Strides Pharma Science

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    Brand Name : Medpro-Ciprofloxacin 750

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    Regulatory Info : Deregistered

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    Brand Name : Aurorix

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    Approval Date : 07/04/2020

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    Regulatory Info : Approved

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    Brand Name : Aurorix

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    Approval Date : 17/12/2019

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    Brand Name : Aurorix

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    Approval Date : 06/11/2019

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    Regulatory Info : Deregistered

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    Moclobemide

    Brand Name : Aurorix

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    Approval Date : 10/03/2000

    Application Number : 20000310000022

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    Regulatory Info : Deregistered

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    Brand Name : Aurorix

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    Approval Date : 17/05/2002

    Application Number : 20020517000328

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    Regulatory Info : Deregistered

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    Brand Name : Aurorix

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    Dosage Strength : 150mg

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    Approval Date : 16/06/2000

    Application Number : 20000616000054

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    ORIFARM GROUP AS

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    ORIFARM GROUP AS

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    Regulatory Info : Deregistered

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    Brand Name : Aurorix

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    Dosage Strength : 300mg

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    Approval Date : 17/05/2002

    Application Number : 20020517000335

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    11

    ORIFARM GROUP AS

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    Brand Name : Aurorix

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    Approval Date : 31/05/2002

    Application Number : 20020531000137

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    Brand Name : PMS-MOCLOBEMIDE

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    Regulatory Info : Prescription

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    Moclobemide

    Brand Name : PMS-MOCLOBEMIDE

    Dosage Form : TABLET

    Dosage Strength : 150MG

    Packaging : 100/500

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    Regulatory Info : Prescription

    Registration Country : Canada

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    Unimedic AB

    Sweden
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    Unimedic AB

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    Regulatory Info : Deregistered

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    Moclobemide

    Brand Name : Aurorix

    Dosage Form : Tablet

    Dosage Strength : 150mg

    Packaging :

    Approval Date : 30/11/2001

    Application Number : 20011130000055

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Unimedic AB

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    Regulatory Info : Deregistered

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    Moclobemide

    Brand Name : Aurorix

    Dosage Form : Tablet

    Dosage Strength : 300mg

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    Approval Date : 30/11/2001

    Application Number : 20011130000062

    Regulatory Info : Deregistered

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    Viatris

    U.S.A
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    Regulatory Info : Approved

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    Moclobemide

    Brand Name : Aurorix

    Dosage Form : Film Coated Tablet

    Dosage Strength : 150mg

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    Approval Date : 08/12/1989

    Application Number : 19891208000118

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    Registration Country : Sweden

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    Paranova Pharmaceuticals Ab

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    Regulatory Info : Deregistered

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    Moclobemide

    Brand Name : Aurorix

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    Approval Date : 30/07/1999

    Application Number : 19990730000051

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Paranova Pharmaceuticals Ab

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    Regulatory Info : Deregistered

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    Brand Name : Aurorix

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    Approval Date : 30/07/1999

    Application Number : 19990730000075

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    Paranova Pharmaceuticals Ab

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    Regulatory Info : Deregistered

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    Moclobemide

    Brand Name : Aurorix

    Dosage Form : Tablet

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    Approval Date : 30/07/1999

    Application Number : 19990730000068

    Regulatory Info : Deregistered

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    Meda Ab

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    Meda Ab

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    Regulatory Info : Deregistered

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    Moclobemide

    Brand Name : Aurorix

    Dosage Form : Film Coated Tablet

    Dosage Strength : 300mg

    Packaging :

    Approval Date : 25/03/1994

    Application Number : 19940325000096

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.