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    Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.

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    Brand Name : FENOFIBRATE

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    Brand Name : FENOFIBRATE

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    Regulatory Info : RX

    Registration Country : USA

    FENOFIBRATE

    AustarPharma

    Dosage Form : TABLET;ORAL

    Brand Name : FENOFIBRATE

    Dosage Strength : 54MG

    Packaging :

    Approval Date : 2017-12-19

    Application Number : 207803

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FENOFIBRATE

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    Brand Name : FENOFIBRATE

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    Regulatory Info : RX

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    FENOFIBRATE

    AustarPharma

    Dosage Form : TABLET;ORAL

    Brand Name : FENOFIBRATE

    Dosage Strength : 160MG

    Packaging :

    Approval Date : 2017-12-19

    Application Number : 207803

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : FENOFIBRATE

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    FENOFIBRATE

    AustarPharma

    Dosage Form : TABLET;ORAL

    Brand Name : FENOFIBRATE

    Dosage Strength : 48MG

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    Approval Date : 2021-02-10

    Application Number : 208476

    Regulatory Info : RX

    Registration Country : USA

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    FENOFIBRATE

    AustarPharma

    Dosage Form : TABLET;ORAL

    Brand Name : FENOFIBRATE

    Dosage Strength : 145MG

    Packaging :

    Approval Date : 2021-02-10

    Application Number : 208476

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : SOLIFENACIN SUCCINAT...

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    Regulatory Info : RX

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    SOLIFENACIN SUCCINATE

    AustarPharma

    Dosage Form : TABLET;ORAL

    Brand Name : SOLIFENACIN SUCCINATE

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 2019-05-20

    Application Number : 210281

    Regulatory Info : RX

    Registration Country : USA

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    Brand Name : SOLIFENACIN SUCCINAT...

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    Brand Name : SOLIFENACIN SUCCINAT...

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    Pharma, Lab & Chemical Expo
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    Regulatory Info : RX

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    SOLIFENACIN SUCCINATE

    AustarPharma

    Dosage Form : TABLET;ORAL

    Brand Name : SOLIFENACIN SUCCINATE

    Dosage Strength : 10MG

    Packaging :

    Approval Date : 2019-05-20

    Application Number : 210281

    Regulatory Info : RX

    Registration Country : USA

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