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    Catalyst Pharmaceuticals

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    01 1AMIFAMPRIDINE PHOSPHATE

    02 7PERAMPANEL

    03 1VAMOROLONE

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    01

    Brand Name : FIRDAPSE

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FIRDAPSE

    U.S.A
    Medlab Asia & Asia Health
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    RLD : Yes

    TE Code :

    AMIFAMPRIDINE PHOSPHATE

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FIRDAPSE

    Dosage Strength : EQ 10MG BASE

    Approval Date : 2018-11-28

    Application Number : 208078

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    02

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 2MG

    Approval Date : 2012-10-22

    Application Number : 202834

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    03

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 4MG

    Approval Date : 2012-10-22

    Application Number : 202834

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 6MG

    Approval Date : 2012-10-22

    Application Number : 202834

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    05

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 8MG

    Approval Date : 2012-10-22

    Application Number : 202834

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    06

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 10MG

    Approval Date : 2012-10-22

    Application Number : 202834

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

    blank

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    Market
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    07

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    • fda
    • EDQM
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 12MG

    Approval Date : 2012-10-22

    Application Number : 202834

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    08

    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : FYCOMPA

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    • fda
    • EDQM
    • WHO-GMP
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    RLD : Yes

    TE Code :

    PERAMPANEL

    Catalyst Pharmaceuticals

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : FYCOMPA

    Dosage Strength : 0.5MG/ML

    Approval Date : 2016-04-29

    Application Number : 208277

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    09

    Brand Name : AGAMREE

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    Brand Name : AGAMREE

    U.S.A
    Medlab Asia & Asia Health
    Not Confirmed
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    • fda
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    RLD : Yes

    TE Code :

    VAMOROLONE

    Catalyst Pharmaceuticals

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : AGAMREE

    Dosage Strength : 40MG/ML

    Approval Date : 2023-10-26

    Application Number : 215239

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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