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    Flumethasone Pivalate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

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    01 1Amdipharm Mercury Company Limited

    02 2ENDO OPERATIONS LTD.

    03 1Hi Pharm

    04 1Novartis Pharmaceuticals Corporation

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    01

    Amdipharm Mercury Company Limited

    United Kingdom
    FNCE
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    Amdipharm Mercury Company Limited

    United Kingdom
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    Regulatory Info : Approved

    Registration Country : Sweden

    Flumethasone Pivalate; Clioquinol

    Brand Name : Locacorten-Vioform

    Dosage Form : Ear Drops

    Dosage Strength : 0.2mg/ml;10mg/ml

    Packaging :

    Approval Date : 17/04/1970

    Application Number : 19700417000027

    Regulatory Info : Approved

    Registration Country : Sweden

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    02

    Hi Pharm

    Egypt
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    Hi Pharm

    Egypt
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    Regulatory Info :

    Registration Country : Egypt

    Flumethasone Pivalate

    Brand Name : Otocort

    Dosage Form : Ear Drop

    Dosage Strength : 10MG

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Egypt

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    03

    Novartis Pharmaceuticals Corporatio...

    Switzerland
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    Regulatory Info : DISCN

    Registration Country : USA

    FLUMETHASONE PIVALATE

    Brand Name : LOCORTEN

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 0.03%

    Packaging :

    Approval Date : 1982-01-01

    Application Number : 16379

    Regulatory Info : DISCN

    Registration Country : USA

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    04

    ENDO OPERATIONS LTD.

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    Regulatory Info : Prescription

    Registration Country : Canada

    FLUMETHASONE PIVALATE

    Brand Name : LOCACORTEN VIOFORM

    Dosage Form : CREAM

    Dosage Strength : 0.02%/W/W

    Packaging :

    Approval Date :

    Application Number : 74462

    Regulatory Info : Prescription

    Registration Country : Canada

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    05

    ENDO OPERATIONS LTD.

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    Regulatory Info : Prescription

    Registration Country : Canada

    FLUMETHASONE PIVALATE

    Brand Name : LOCACORTEN VIOFORM EARDROPS

    Dosage Form : DROPS

    Dosage Strength : 0.02%/W/V

    Packaging : 10ML

    Approval Date :

    Application Number : 74454

    Regulatory Info : Prescription

    Registration Country : Canada

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