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    Approval Date : 22-03-2018

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    Approval Date : 04-05-2011

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    United Kingdom
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    Approval Date : 30/09/1997

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    Regulatory Info : Approved

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    Approval Date : 10-03-1997

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    GSK

    United Kingdom
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    Naratriptan Hydrochloride

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    Approval Date : 01-06-2001

    Application Number : 2.00E+13

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    Orchid Pharma

    India
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    Regulatory Info : Generic EU CTD

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    ORIFARM GROUP AS

    Denmark
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    Naratriptan Hydrochloride

    Brand Name : Naramig

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    Approval Date : 26-03-2003

    Application Number : 2.00E+13

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    11

    ORIFARM GROUP AS

    Denmark
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    Regulatory Info : Deregistered

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    Naratriptan Hydrochloride

    Brand Name : Naramig

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    Approval Date : 09-04-2003

    Application Number : 2.00E+13

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    ORIFARM GROUP AS

    Denmark
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    Regulatory Info : Deregistered

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    Naratriptan Hydrochloride

    Brand Name : Naramig

    Dosage Form : Film Coated Tablet

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    Approval Date : 04-03-2004

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

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    ORIFARM GROUP AS

    Denmark
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    Regulatory Info : Deregistered

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    Naratriptan Hydrochloride

    Brand Name : Naramig

    Dosage Form : Film Coated Tablet

    Dosage Strength : 2.5mg

    Packaging :

    Approval Date : 24-05-2017

    Application Number : 2.02E+13

    Regulatory Info : Deregistered

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    14

    ORIFARM GROUP AS

    Denmark
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    Denmark
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    Regulatory Info : Deregistered

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    Naratriptan Hydrochloride

    Brand Name : Naramig

    Dosage Form : Film Coated Tablet

    Dosage Strength : 2.5mg

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    Approval Date : 28-06-2017

    Application Number : 2.02E+13

    Regulatory Info : Deregistered

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    ORIFARM GROUP AS

    Denmark
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    Regulatory Info : Approved

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    Naratriptan Hydrochloride

    Brand Name : Naratriptan Orifarm

    Dosage Form : Film Coated Tablet

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    Approval Date : 23-02-2018

    Application Number : 2.02E+13

    Regulatory Info : Approved

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    Renata Limited

    Bangladesh
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    Regulatory Info : Authorised

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    Naratriptan

    Brand Name : Naratriptan

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    Approval Date : 2024-02-28

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    Regulatory Info : Authorised

    Registration Country : Malta

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    Teva Pharmaceutical Industries

    Israel
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    Israel
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    Regulatory Info : Withdrawn

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    Naratriptan

    Brand Name : Naraverg

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    Approval Date : 2011-09-27

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    Regulatory Info : Withdrawn

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    Paranova Pharmaceuticals Ab

    Country
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    Regulatory Info : Deregistered

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    Naratriptan Hydrochloride

    Brand Name : Naramig

    Dosage Form : Film Coated Tablet

    Dosage Strength : 2.5mg

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    Approval Date : 11-01-2002

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

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    Ivax Scandinavia Ab

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    Regulatory Info : Deregistered

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    Naratriptan Hydrochloride

    Brand Name : Naramig

    Dosage Form : Film Coated Tablet

    Dosage Strength : 2.5mg

    Packaging :

    Approval Date : 29-11-2002

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Paranova Pharmaceuticals Ab

    Country
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Naratriptan Hydrochloride

    Brand Name : Naramig

    Dosage Form : Film Coated Tablet

    Dosage Strength : 2.5mg

    Packaging :

    Approval Date : 06-04-2005

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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