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    Axsome Therapeutics

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    01 2BUPROPION HYDROCHLORIDE; DEXTROMETHORPHAN HYDROBROMIDE

    02 1MELOXICAM; RIZATRIPTAN BENZOATE

    03 2SOLRIAMFETOL HYDROCHLORIDE

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    01

    Brand Name : AUVELITY

    U.S.A
    PEGS Boston Summit
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    Brand Name : AUVELITY

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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 : AUVELITY

    U.S.A
    PEGS Boston Summit
    Not Confirmed
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    Brand Name : AUVELITY

    U.S.A
    PEGS Boston Summit
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    • EDQM
    • WHO-GMP
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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;30MG

    Approval Date : 2026-04-30

    Application Number : 215430

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : SYMBRAVO

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    RLD : Yes

    TE Code :

    MELOXICAM; RIZATRIPTAN BENZOATE

    Axsome Therapeutics

    Dosage Form : TABLET; ORAL

    Proprietary Name : SYMBRAVO

    Dosage Strength : 20MG;EQ 10MG BASE

    Approval Date : 2025-01-30

    Application Number : 215431

    RX/OTC/DISCN : RX

    RLD : Yes

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    04

    Brand Name : SUNOSI

    U.S.A
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    Brand Name : SUNOSI

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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

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    05

    Brand Name : SUNOSI

    U.S.A
    PEGS Boston Summit
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    Brand Name : SUNOSI

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    PEGS Boston Summit
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    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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    • 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.