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    [1-(1-adamantyl)ethyl]amine hydrochloride

    ACTIVE PHARMA INGREDIENTS

    INTERMEDIATES

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    01 1CHARTWELL RX

    02 1FOREST LABS

    03 1IMPAX LABS

    04 1IMPAX LABS INC

    05 1SUN PHARM INDS INC

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    01

    CHARTWELL RX

    U.S.A
    Compamed
    Not Confirmed
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    CHARTWELL RX

    U.S.A
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    Compamed
    Not Confirmed
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    RLD : No

    TE Code :

    RIMANTADINE HYDROCHLORIDE

    Brand Name : RIMANTADINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 2003-01-14

    Application Number : 76375

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    FOREST LABS

    U.S.A
    Compamed
    Not Confirmed
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    FOREST LABS

    U.S.A
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    Compamed
    Not Confirmed
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    RLD : No

    TE Code :

    RIMANTADINE HYDROCHLORIDE

    Brand Name : FLUMADINE

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 50MG/5ML

    Approval Date : 1993-09-17

    Application Number : 19650

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    IMPAX LABS INC

    U.S.A
    Compamed
    Not Confirmed
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    IMPAX LABS INC

    U.S.A
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    RLD : No

    TE Code :

    RIMANTADINE HYDROCHLORIDE

    Brand Name : RIMANTADINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 2001-11-02

    Application Number : 75916

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    IMPAX LABS

    U.S.A
    Compamed
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    IMPAX LABS

    U.S.A
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    RLD : No

    TE Code :

    RIMANTADINE HYDROCHLORIDE

    Brand Name : RIMANTADINE HYDROCHLORIDE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 2002-08-30

    Application Number : 76132

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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    05

    SUN PHARM INDS INC

    India
    Compamed
    Not Confirmed
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    SUN PHARM INDS INC

    India
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    RLD : Yes

    TE Code :

    RIMANTADINE HYDROCHLORIDE

    Brand Name : FLUMADINE

    Dosage Form : TABLET;ORAL

    Dosage Strength : 100MG

    Approval Date : 1993-09-17

    Application Number : 19649

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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