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    Avondale Pharmaceutical

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    FINISHED DOSAGE FORMULATIONS

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    01 2DIFLORASONE DIACETATE

    02 1MELOXICAM

    03 1NIACIN

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    01

    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
    arrow
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    • WHO-GMP
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    RLD : No

    TE Code :

    DIFLORASONE DIACETATE

    Avondale Pharmaceutical

    Dosage Form : CREAM; TOPICAL

    Proprietary Name : DIFLORASONE DIACETATE

    Dosage Strength : 0.05%

    Approval Date : 1998-03-30

    Application Number : 75187

    RX/OTC/DISCN : DISCN

    RLD : No

    TE Code :

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    02

    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
    arrow

    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
    arrow
    • 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 : AB

    DIFLORASONE DIACETATE

    Avondale Pharmaceutical

    Dosage Form : OINTMENT; TOPICAL

    Proprietary Name : DIFLORASONE DIACETATE

    Dosage Strength : 0.05%

    Approval Date : 1999-04-27

    Application Number : 75374

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : MELOXICAM

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Brand Name : MELOXICAM

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    • WHO-GMP
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    RLD : Yes

    TE Code :

    MELOXICAM

    Avondale Pharmaceutical

    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : MELOXICAM

    Dosage Strength : 7.5MG/5ML

    Approval Date : 2004-06-01

    Application Number : 21530

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code :

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    04

    Brand Name : NIACOR

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    Brand Name : NIACOR

    U.S.A
    euroPLX 86 Munich
    Not Confirmed
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    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code :

    NIACIN

    Avondale Pharmaceutical

    Dosage Form : TABLET; ORAL

    Proprietary Name : NIACOR

    Dosage Strength : 500MG

    Approval Date : 2000-05-03

    Application Number : 40378

    RX/OTC/DISCN : RX

    RLD : No

    TE Code :

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