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    Triamcinolone Diacetate

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    Triamcinolone Diacetate

    ACTIVE PHARMA INGREDIENTS

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    01 2Actavis Inc

    02 1Aldo-Union

    03 1Astellas Pharma

    04 1DELCOR ASSET

    05 2Epic Pharma. LLC.

    06 2Fosun Pharmaceutical

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    01

    Actavis Inc

    Ireland
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : TRIAMCINOLONE DIACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 84072

    Regulatory Info : DISCN

    Registration Country : USA

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    02

    Actavis Inc

    Ireland
    BioJapan
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    Actavis Inc

    Ireland
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    BioJapan
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : TRIAMCINOLONE DIACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85529

    Regulatory Info : DISCN

    Registration Country : USA

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    03

    Aldo-Union

    Spain
    BioJapan
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    Aldo-Union

    Spain
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    Regulatory Info : Authorized

    Registration Country : Spain

    Triamcinolone Diacetate

    Brand Name : Proctosteroid

    Dosage Form : Rectal Foam

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 1984-04-01

    Application Number : 55845

    Regulatory Info : Authorized

    Registration Country : Spain

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    04

    Astellas Pharma

    Japan
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    Astellas Pharma

    Japan
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : ARISTOCORT

    Dosage Form : SYRUP;ORAL

    Dosage Strength : 2MG/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11960

    Regulatory Info : DISCN

    Registration Country : USA

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    05

    DELCOR ASSET

    U.S.A
    BioJapan
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    DELCOR ASSET

    U.S.A
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    BioJapan
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : KENACORT

    Dosage Form : SYRUP;ORAL

    Dosage Strength : EQ 4MG BASE/5ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12515

    Regulatory Info : DISCN

    Registration Country : USA

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    06

    Epic Pharma. LLC.

    U.S.A
    BioJapan
    Not Confirmed
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    Epic Pharma. LLC.

    U.S.A
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    BioJapan
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : TRIAMCINOLONE DIACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 85122

    Regulatory Info : DISCN

    Registration Country : USA

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    07

    Epic Pharma. LLC.

    U.S.A
    BioJapan
    Not Confirmed
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    Epic Pharma. LLC.

    U.S.A
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    BioJapan
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : TRIAMCINOLONE DIACETATE

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 86394

    Regulatory Info : DISCN

    Registration Country : USA

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    08

    Fosun Pharmaceutical

    China
    BioJapan
    Not Confirmed
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    Fosun Pharmaceutical

    China
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    BioJapan
    Not Confirmed
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : ARISTOCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 25MG/ML

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 11685

    Regulatory Info : DISCN

    Registration Country : USA

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    09

    Fosun Pharmaceutical

    China
    BioJapan
    Not Confirmed
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    Fosun Pharmaceutical

    China
    arrow
    BioJapan
    Not Confirmed
    • fda
    • EDQM
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    Regulatory Info : DISCN

    Registration Country : USA

    TRIAMCINOLONE DIACETATE

    Brand Name : ARISTOCORT

    Dosage Form : INJECTABLE;INJECTION

    Dosage Strength : 40MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 12802

    Regulatory Info : DISCN

    Registration Country : USA

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