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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
    The Generic Rx Session
    Not Confirmed
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    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
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    The Generic Rx Session
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    DIFLORASONE DIACETATE

    Avondale Pharmaceutical

    Dosage Form : CREAM;TOPICAL

    Brand Name : DIFLORASONE DIACETATE

    Dosage Strength : 0.05%

    Packaging :

    Approval Date : 1998-03-30

    Application Number : 75187

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
    The Generic Rx Session
    Not Confirmed
    arrow

    Brand Name : DIFLORASONE DIACETAT...

    U.S.A
    arrow
    The Generic Rx Session
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
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    Regulatory Info : RX

    Registration Country : USA

    DIFLORASONE DIACETATE

    Avondale Pharmaceutical

    Dosage Form : OINTMENT;TOPICAL

    Brand Name : DIFLORASONE DIACETATE

    Dosage Strength : 0.05%

    Packaging :

    Approval Date : 1999-04-27

    Application Number : 75374

    Regulatory Info : RX

    Registration Country : USA

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    03

    Brand Name : MELOXICAM

    U.S.A
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    Brand Name : MELOXICAM

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    BioAsia
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    Regulatory Info : RX

    Registration Country : USA

    MELOXICAM

    Avondale Pharmaceutical

    Dosage Form : SUSPENSION;ORAL

    Brand Name : MELOXICAM

    Dosage Strength : 7.5MG/5ML

    Packaging :

    Approval Date : 2004-06-01

    Application Number : 21530

    Regulatory Info : RX

    Registration Country : USA

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    04

    Brand Name : NIACOR

    U.S.A
    The Generic Rx Session
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    Brand Name : NIACOR

    U.S.A
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    The Generic Rx Session
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    Regulatory Info : RX

    Registration Country : USA

    NIACIN

    Avondale Pharmaceutical

    Dosage Form : TABLET;ORAL

    Brand Name : NIACOR

    Dosage Strength : 500MG

    Packaging :

    Approval Date : 2000-05-03

    Application Number : 40378

    Regulatory Info : RX

    Registration Country : USA

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