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    AbbVie Inc

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    MEMANTINE HYDROCHLORIDE

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    Approval Date : 2003-10-16

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    Allergan Aesthetics

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    MEMANTINE HYDROCHLORIDE

    Brand Name : NAMENDA

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    Dosage Strength : 2MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2005-04-18

    Application Number : 21627

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    Orion Corporation

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    Regulatory Info : Deregistered

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    Memantine Hydrochloride

    Brand Name : Memantin Orion

    Dosage Form : Film Coated Tablet

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    Approval Date : 22/03/2013

    Application Number : 20120523000029

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    Memantine Hydrochloride

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    Memantine Hydrochloride

    Brand Name : Cognimet 10

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    Emay Pharmaceuticals

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    Memantine Hydrochloride

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    Dosage Form : Pellets

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    Alfred E Tiefenbacher GmbH

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    Virtual BoothWe are the TIEFENBACHER GROUP, Health Pioneers since 1963.

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    Memantine Hydrochloride

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    Virtual BoothPharmathen provides life cycle Management solutions for branded pharma, as well as to develop & establish new technology platforms.

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    Regulatory Info : EU Approved

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    Memantine Hydrochloride

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    Strides Pharma Science

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    Virtual BoothSynergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.

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    MEMANTINE HYDROCHLORIDE

    Brand Name : MEMANTINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 5MG

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    Approval Date : 2017-05-23

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    Towa Pharmaceutical

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    Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

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    Regulatory Info : Authorized

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    Memantine Hydrochloride

    Brand Name : Memantina Pensa

    Dosage Form : Film Coated Tablet

    Dosage Strength : 20MG

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    Approval Date : 2013-12-16

    Application Number : 78320

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    AbbVie Inc

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    MEMANTINE HYDROCHLORIDE

    Brand Name : NAMENDA

    Dosage Form : TABLET;ORAL

    Dosage Strength : 10MG

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    Approval Date : 2003-10-16

    Application Number : 21487

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    AbbVie Inc

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    MEMANTINE HYDROCHLORIDE

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    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 7MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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    Approval Date : 2010-06-21

    Application Number : 22525

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    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 14MG

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    Approval Date : 2010-06-21

    Application Number : 22525

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    MEMANTINE HYDROCHLORIDE

    Brand Name : NAMENDA XR

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 21MG

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    Approval Date : 2010-06-21

    Application Number : 22525

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    Brand Name : NAMENDA XR

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 28MG

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    Approval Date : 2010-06-21

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    DONEPEZIL HYDROCHLORIDE; MEMANTINE HYDROCHLORIDE

    Brand Name : NAMZARIC

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG;14MG

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    Approval Date : 2014-12-23

    Application Number : 206439

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    Brand Name : NAMZARIC

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG;28MG

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    Approval Date : 2014-12-23

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    Brand Name : NAMZARIC

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG;7MG

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    Approval Date : 2016-07-18

    Application Number : 206439

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    AbbVie Inc

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    Brand Name : NAMZARIC

    Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL

    Dosage Strength : 10MG;21MG

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    Approval Date : 2016-07-18

    Application Number : 206439

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    Orion Corporation

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    Regulatory Info : Deregistered

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    Memantine Hydrochloride

    Brand Name : Memantin Orion

    Dosage Form : Film Coated Tablet

    Dosage Strength : 20mg

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    Approval Date : 22/03/2013

    Application Number : 20120523000036

    Regulatory Info : Deregistered

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