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    Biperiden Hydrochloride

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    01 2Laboratorio Farmaceutica SIT Srl

    02 3Pharmaceutical Laboratory Sit - Hygienic Therapeutic Specialties Srl

    03 3SIT LABORATORIO FARMAC. Srl

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    Laboratorio Farmaceutica SIT Srl

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    Regulatory Info : Not Marketed

    Registration Country : Norway

    Biperiden hydrochloride

    Brand Name : Akineton

    Dosage Form : Tablet

    Dosage Strength : 2mg

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    Regulatory Info : Not Marketed

    Registration Country : Norway

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    Regulatory Info : Marketed

    Registration Country : Norway

    Biperiden hydrochloride

    Brand Name : Akineton

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    Registration Country : Italy

    Biperiden

    Brand Name : Akineton

    Dosage Form : Biperiden 2Mg 60 Units Oral Use

    Dosage Strength : 60 CPR 2 mg

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    Registration Country : Italy

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    Registration Country : Italy

    Biperiden

    Brand Name : Akineton

    Dosage Form : Biperiden 4Mg 50 Combined Oral Use Rp

    Dosage Strength : 50 CPR 4 mg prolonged release

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    Registration Country : Italy

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    Registration Country : Italy

    Biperiden

    Brand Name : Akineton

    Dosage Form : Biperiden 5Mg 5 Units Parenteral Use

    Dosage Strength : 5 VIALS IM EV 5 mg 1 ml

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    Registration Country : Italy

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    Regulatory Info : Authorized

    Registration Country : Spain

    Biperideno Hydrochloride

    Brand Name : Akineton

    Dosage Form : Tablet

    Dosage Strength : 2MG

    Packaging :

    Approval Date : 1956-11-01

    Application Number : 26692

    Regulatory Info : Authorized

    Registration Country : Spain

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    Regulatory Info : Authorized

    Registration Country : Spain

    Biperideno Hydrochloride

    Brand Name : Akineton Retard

    Dosage Form : Extended-Release Tablet

    Dosage Strength : 4MG

    Packaging :

    Approval Date : 1973-05-01

    Application Number : 51224

    Regulatory Info : Authorized

    Registration Country : Spain

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    Regulatory Info : Authorized

    Registration Country : Spain

    Biperidene

    Brand Name : Akineton

    Dosage Form : Injectable Solution

    Dosage Strength : 5MG

    Packaging :

    Approval Date : 1958-03-01

    Application Number : 28994

    Regulatory Info : Authorized

    Registration Country : Spain

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