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    Aspen API. More than just an API™

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    Sharp is a leader in commercial packaging, clinical services, and sterile manufacturing.

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    Suanfarma, at the Core of a Better Life.

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    ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.

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    Amoxicillin Sodium

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    05 1Apotex Europe Bv

    06 4Aurovitas Spain, Sau

    07 1Bexal Farmaceutica Sa

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    27 7Sandoz Pharmaceuticals Sa

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    33 1Tarchominskie Zaklady Farmaceutyczne „Polfa” Spólka Akcyjna

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    Towa Pharmaceutical Sa

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    Virtual BoothTowa Pharma is dedicated to researching, developing, producing, and promoting generic drugs.

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    Regulatory Info : Suspended

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    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilina/Acido Clavulanico Pensa Pharma

    Dosage Form : Film Coated Tablet

    Dosage Strength : 500MG; 125 MG

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    Approval Date : 30-05-2019

    Application Number : 84183

    Regulatory Info : Suspended

    Registration Country : Spain

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    Towa Pharmaceutical Sa

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    Regulatory Info : Authorized

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    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilina/Acido Clavulanico Pensa Pharma

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875MG; 125 MG

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    Approval Date : 30-05-2019

    Application Number : 84184

    Regulatory Info : Authorized

    Registration Country : Spain

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    Regulatory Info : Prescription

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    Amoxicillin Sodium; Clavulanate Potassium

    Brand Name : Medoclav

    Dosage Form : Injection/Infusion Solution

    Dosage Strength : 1000mg; 200mg

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    Approval Date : 31-05-2024

    Application Number : 28107164824

    Regulatory Info : Prescription

    Registration Country : Denmark

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    Antibiotice S.A.

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    Regulatory Info : Authorised

    Registration Country : Malta

    Clavulanate Potassium; Amoxicillin Sodium

    Brand Name : Amoxiplus

    Dosage Form : Powder For Solution For Injection And Infusion

    Dosage Strength : 200MG; 1000MG

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    Approval Date : 2024-09-25

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    Regulatory Info : Authorised

    Registration Country : Malta

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    Apotex Europe Bv

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    Regulatory Info : Cancelled

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    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilin/Clavulanic Acid Apotex

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875MG; 125 MG

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    Approval Date : 05-05-2003

    Application Number : 65356

    Regulatory Info : Cancelled

    Registration Country : Spain

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    Alter Laboratories Sa

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    Regulatory Info : Authorized

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    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilin/Clavulanic Acid Alter

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875MG; 125 MG

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    Approval Date : 24-05-2013

    Application Number : 77533

    Regulatory Info : Authorized

    Registration Country : Spain

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    Aurovitas Spain, Sau

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    Regulatory Info : Authorized

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    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilin/Clavulanic Acid Aurovitas Pharma

    Dosage Form : Tablet

    Dosage Strength : 500MG; 125 MG

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    Approval Date : 11-02-2010

    Application Number : 71886

    Regulatory Info : Authorized

    Registration Country : Spain

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    Aurovitas Spain, Sau

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    Regulatory Info : Authorized

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    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilin/Clavulanic Acid Aurovitas Pharma

    Dosage Form : Tablet

    Dosage Strength : 875MG; 125 MG

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    Approval Date : 11-02-2010

    Application Number : 71887

    Regulatory Info : Authorized

    Registration Country : Spain

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    09

    Aurovitas Spain, Sau

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    Regulatory Info : Authorized

    Registration Country : Spain

    Amoxicil Trihydrate; Potase Clavulanate

    Brand Name : Amoxicilin/Clavulanic Acid Aurovitas

    Dosage Form : Film Coated Tablet

    Dosage Strength : 875MG; 125 MG

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    Approval Date : 19-10-2018

    Application Number : 83523

    Regulatory Info : Authorized

    Registration Country : Spain

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    Aurovitas Spain, Sau

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    Regulatory Info : Authorized

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    Amoxicilin Trihydrate; Clavulanic Acid

    Brand Name : Amoxicilina/Acid Clavulanico Aurovitas

    Dosage Form : Powder For Oral Suspension In Sachet

    Dosage Strength : 875MG; 125 MG

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    Approval Date : 03-11-2023

    Application Number : 89132

    Regulatory Info : Authorized

    Registration Country : Spain

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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.