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    Axsome Therapeutics

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    01 1BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE

    02 2SOLRIAMFETOL HYDROCHLORIDE

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    01

    Brand Name : AUVELITY

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    Brand Name : AUVELITY

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
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    RLD : Yes

    TE Code :

    BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE

    Axsome Therapeutics

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : AUVELITY

    Dosage Strength : 105MG;45MG

    Approval Date : 2022-08-18

    Application Number : 215430

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : SUNOSI

    U.S.A
    Pharmtech & Ingredients
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    Brand Name : SUNOSI

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    RLD : Yes

    TE Code :

    SOLRIAMFETOL HYDROCHLORIDE

    Axsome Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : SUNOSI

    Dosage Strength : EQ 75MG BASE

    Approval Date : 2019-06-17

    Application Number : 211230

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : SUNOSI

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow

    Brand Name : SUNOSI

    U.S.A
    Pharmtech & Ingredients
    Not Confirmed
    arrow
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
    Post an Enquiry Post an Enquiry
    Flag U.S.A
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : Yes

    TE Code :

    SOLRIAMFETOL HYDROCHLORIDE

    Axsome Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : SUNOSI

    Dosage Strength : EQ 150MG BASE

    Approval Date : 2019-06-17

    Application Number : 211230

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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