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    Approved Drug Products containing Oxtriphylline listed in the FDA Orange Book. Original Data : FDA Website

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    Oxtriphylline

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    DIGITAL CONTENT

    MARKET PLACE

    REF. STANDARDS & IMPURITIES

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    01 2MORTON GROVE

    02 4PARKE DAVIS

    03 2WARNER CHILCOTT LLC

    04 2WATSON LABS

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    01

    WATSON LABS

    Ireland
    FNCE 2024
    Not Confirmed
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    WATSON LABS

    Ireland
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : OXTRIPHYLLINE

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 200MG

    Approval Date : 1983-08-25

    Application Number : 87835

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    WATSON LABS

    Ireland
    FNCE 2024
    Not Confirmed
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    WATSON LABS

    Ireland
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : OXTRIPHYLLINE

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1983-08-25

    Application Number : 87866

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    MORTON GROVE

    U.S.A
    FNCE 2024
    Not Confirmed
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    MORTON GROVE

    U.S.A
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : OXTRIPHYLLINE PEDIATRIC

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 50MG/5ML

    Approval Date : 1983-12-05

    Application Number : 88242

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    MORTON GROVE

    U.S.A
    FNCE 2024
    Not Confirmed
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    MORTON GROVE

    U.S.A
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    FNCE 2024
    Not Confirmed
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : OXTRIPHYLLINE

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 100MG/5ML

    Approval Date : 1983-12-05

    Application Number : 88243

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    05

    PARKE DAVIS

    U.S.A
    FNCE 2024
    Not Confirmed
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    PARKE DAVIS

    U.S.A
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : CHOLEDYL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 100MG

    Approval Date : 1982-01-01

    Application Number : 9268

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    06

    PARKE DAVIS

    U.S.A
    FNCE 2024
    Not Confirmed
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    PARKE DAVIS

    U.S.A
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    FNCE 2024
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : CHOLEDYL

    Dosage Form : TABLET, DELAYED RELEASE;ORAL

    Dosage Strength : 200MG

    Approval Date : 1982-01-01

    Application Number : 9268

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    07

    PARKE DAVIS

    U.S.A
    FNCE 2024
    Not Confirmed
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    PARKE DAVIS

    U.S.A
    arrow
    FNCE 2024
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : CHOLEDYL

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 50MG/5ML

    Approval Date : 1982-01-01

    Application Number : 9268

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    PARKE DAVIS

    U.S.A
    FNCE 2024
    Not Confirmed
    arrow

    PARKE DAVIS

    U.S.A
    arrow
    FNCE 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : CHOLEDYL

    Dosage Form : SOLUTION;ORAL

    Dosage Strength : 100MG/5ML

    Approval Date : 1984-11-27

    Application Number : 9268

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    WARNER CHILCOTT LLC

    U.S.A
    FNCE 2024
    Not Confirmed
    arrow

    WARNER CHILCOTT LLC

    U.S.A
    arrow
    FNCE 2024
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : CHOLEDYL SA

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 600MG

    Approval Date : 1982-01-01

    Application Number : 86742

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    10

    WARNER CHILCOTT LLC

    U.S.A
    FNCE 2024
    Not Confirmed
    arrow

    WARNER CHILCOTT LLC

    U.S.A
    arrow
    FNCE 2024
    Not Confirmed
    • 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 : No

    TE Code :

    OXTRIPHYLLINE

    Brand Name : CHOLEDYL SA

    Dosage Form : TABLET, EXTENDED RELEASE;ORAL

    Dosage Strength : 400MG

    Approval Date : 1983-05-24

    Application Number : 87863

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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