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    Tox21_202988

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    RELATED EXCIPIENT COMPANIES

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    GLOBAL SALES INFORMATION

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    01 1AMBIX

    02 1LANNETT

    03 2PERRIGO NEW YORK

    04 1SHERWOOD MEDCL

    05 3SHIRE

    06 1SUN PHARMA CANADA

    07 2WENDT

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    01

    AMBIX

    U.S.A
    CTAD25
    Not Confirmed
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    AMBIX

    U.S.A
    arrow
    CTAD25
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : NITROFURAZONE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 86077

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    LANNETT

    U.S.A
    CTAD25
    Not Confirmed
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    LANNETT

    U.S.A
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    CTAD25
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : NITROFURAZONE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 84393

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    03

    PERRIGO NEW YORK

    Ireland
    CTAD25
    Not Confirmed
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    PERRIGO NEW YORK

    Ireland
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    CTAD25
    Not Confirmed
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : NITROFURAZONE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 84968

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    04

    PERRIGO NEW YORK

    Ireland
    CTAD25
    Not Confirmed
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    PERRIGO NEW YORK

    Ireland
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    CTAD25
    Not Confirmed
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : NITROFURAZONE

    Dosage Form : SOLUTION;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 85130

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    05

    SHIRE

    United Kingdom
    CTAD25
    Not Confirmed
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    SHIRE

    United Kingdom
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    CTAD25
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : FURACIN

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 5795

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    06

    SHIRE

    United Kingdom
    CTAD25
    Not Confirmed
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    SHIRE

    United Kingdom
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    CTAD25
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : FURACIN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 83789

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    07

    SHIRE

    United Kingdom
    CTAD25
    Not Confirmed
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    SHIRE

    United Kingdom
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    CTAD25
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : FURACIN

    Dosage Form : POWDER;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 83791

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    08

    WENDT

    Canada
    CTAD25
    Not Confirmed
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    WENDT

    Canada
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    CTAD25
    Not Confirmed
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    • EDQM
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : NITROFURAZONE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 86766

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    09

    SHERWOOD MEDCL

    Country
    CTAD25
    Not Confirmed
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    SHERWOOD MEDCL

    Country
    arrow
    CTAD25
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    NITROFURAZONE

    Brand Name : ACTIN-N

    Dosage Form : DRESSING;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 17343

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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    10

    SUN PHARMA CANADA

    Country
    CTAD25
    Not Confirmed
    arrow

    SUN PHARMA CANADA

    Country
    arrow
    CTAD25
    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 :

    NITROFURAZONE

    Brand Name : NITROFURAZONE

    Dosage Form : OINTMENT;TOPICAL

    Dosage Strength : 0.2%

    Approval Date : 1982-01-01

    Application Number : 86156

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

    blank

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