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    Amoxicillin-Clavulanic Acid

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    01 2Aristo Pharma Gmbh

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    04 2Krka Sweden Ab

    05 1Meda Ab

    06 1Mylan Ab

    07 3Orifarm Ab

    08 2SANDOZ B.V.

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    Aristo Pharma Gmbh

    Germany
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    Aristo Pharma Gmbh

    Germany
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    Regulatory Info : Approved

    Registration Country : Sweden

    Amoxicillin Trihydrate Potassium Clavulanate

    Brand Name : Klaximols

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500mg;125mg

    Packaging :

    Approval Date : 27-01-2012

    Application Number : 2.01E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    02

    Aristo Pharma Gmbh

    Germany
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    Aristo Pharma Gmbh

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    Regulatory Info : Approved

    Registration Country : Sweden

    Amoxicillin Trihydrate Potassium Clavulanate

    Brand Name : Klaximols

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875mg;125mg

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    Approval Date : 27-01-2012

    Application Number : 2.01E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    03

    GLAXOSMITHKLINE SpA

    United Kingdom
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    Regulatory Info :

    Registration Country : Italy

    Co-Amoxiclav

    Brand Name : Augmentin

    Dosage Form : Amoxicillin+Clavulanic Acid+2001,000 Mg 20Ml 1 Units Parenteral Use

    Dosage Strength : 1 ampoule EV 1,000 mg + 200mg + 1 vial solv 20 ml

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    Registration Country : Italy

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    GLAXOSMITHKLINE SpA

    United Kingdom
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    Regulatory Info :

    Registration Country : Italy

    Co-Amoxiclav

    Brand Name : Augmentin

    Dosage Form : Amoxicillin+Clavulanic Acid+2002,000 Mg 1 Unit Parenteral Use

    Dosage Strength : 1 ampoule EV 2,000 mg + 200 mg

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    Registration Country : Italy

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    05

    Krka Sweden Ab

    Slovenia
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    Regulatory Info : Approved

    Registration Country : Sweden

    Amoxicillin Trihydrate Potassium Clavulanate

    Brand Name : Betaclav

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500mg;125mg

    Packaging :

    Approval Date : 20-08-2015

    Application Number : 2.01E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    06

    Krka Sweden Ab

    Slovenia
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    Krka Sweden Ab

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    Regulatory Info : Approved

    Registration Country : Sweden

    Amoxicillin Trihydrate Potassium Clavulanate

    Brand Name : Betaclav

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875mg;125mg

    Packaging :

    Approval Date : 20-08-2015

    Application Number : 2.01E+13

    Regulatory Info : Approved

    Registration Country : Sweden

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    07

    Mylan Ab

    U.S.A
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    Mylan Ab

    U.S.A
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Amoxicillin Trihydrate Potassium Clavulanate

    Brand Name : Amoclav Mylan

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875mg

    Packaging :

    Approval Date : 10-08-2001

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    08

    IBIGEN Srl

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    Regulatory Info :

    Registration Country : Italy

    Co-Amoxiclav

    Brand Name : Amoxycillin And Clavulanic Acid

    Dosage Form : Amoxicillin+Clavulanic Acid+2001,000 Mg 20Ml 1 Units Parenteral Use

    Dosage Strength : 1 vial EV 1,000 mg + 200mg + 1 vial solv 20 ml

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    09

    IBIGEN Srl

    Country
    ASCO GU
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    IBIGEN Srl

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    Regulatory Info :

    Registration Country : Italy

    Co-Amoxiclav

    Brand Name : Amoxycillin And Clavulanic Acid

    Dosage Form : Amoxicillin+Clavulanic Acid+2002,000 Mg 20Ml 1 Units Parenteral Use

    Dosage Strength : 1 ampoule EV 2,000 mg + 200mg + 1 vial solv 20 ml

    Packaging :

    Approval Date :

    Application Number :

    Regulatory Info :

    Registration Country : Italy

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    10

    Meda Ab

    Country
    ASCO GU
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    Meda Ab

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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Amoxicillin Trihydrate Potassium Clavulanate

    Brand Name : Spektramox

    Dosage Form : Film Coated Tablet

    Dosage Strength : 250mg;125mg

    Packaging :

    Approval Date : 19-12-1994

    Application Number : 1.99E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.