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    All Manufacturers, Suppliers, Distributors and Exporters of Amoxicillin Trihydrate with approved in Europe Marketing Authorisations (MA) of Finished Dosage Form listed on PharmaCompass.com

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    Amoxicillin Trihydrate

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    Atabay Kimya Sanayi ve Ticaret A.S.

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    Amoxicillin; Clavulanic Acid

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    Powder for Oral Suspension
    400MG/5ML; 57MG/5ML
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    Amoxicillin; Clavulanic Acid

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    Amoxicillin; Clavulanic Acid

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    Amoxicillin+Clavulanic Acid+11,480 Mg/Ml 140Ml Oral Use
    os suspe grat 140 ml 400 mg/5 ml + 57 mg/5 ml
    Amoxycillin And Clavulanic Acid
    Italy
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    Axapharm AG

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      Amoxicillin Trihydrate; Clavulanic Acid

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      BLUEFISH PHARMACEUTICALS AB

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        Deva Holding AS

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        Amoxicillin Trihydrate; Clavulanic Acid

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        Powder for Oral Suspension
        600MG; 42.9MG
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        Turkey
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        Deva Holding AS

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        Deva Holding AS

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            GLAXOSMITHKLINE SpA

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            Clavulin
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            Amoxicillin+Clavulanic Acid+11,480 Mg/Ml 140Ml Oral Use
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              Sandoz Pharmaceuticals AG

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              Spirig HealthCare AG

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                    Mylan AB

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                    Meda AB

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                    Amoxicillin Trihydrate; Clavulanic Acid

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                    Co-Amoxi Mepha, Trockensub 2200 mg, Durchstf 10 Stk
                    Switzerland
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                    Amoxicillin

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                    Antic-calc Tablet
                    375 mg
                    Imacillin
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                    Norway
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                    Amoxicillin

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                    Antic-calc Tablet
                    500 mg
                    Imacillin
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                    Norway
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                    Amoxicillin

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                    Antic-calc Tablet
                    500 mg
                    Imacillin
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                    Norway
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                    • TABLET;ORAL - 250MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
                    • TABLET;ORAL - 500MG;EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
                    • FOR SUSPENSION;ORAL - 125MG/5ML;EQ 31.25MG BASE/5ML
                    • FOR SUSPENSION;ORAL - 250MG/5ML;EQ 62.5MG BASE/5ML
                    • TABLET;ORAL - 875MG;EQ 125MG BASE
                    • FOR SUSPENSION;ORAL - 200MG/5ML;EQ 28.5MG BASE/5ML
                    • FOR SUSPENSION;ORAL - 400MG/5ML;EQ 57MG BASE/5ML
                    • TABLET;ORAL - 500MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
                    • TABLET;ORAL - 875MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
                    • FOR SUSPENSION;ORAL - 600MG/5ML;EQ 42.9MG BASE/5ML
                    • CAPSULE, TABLET, CAPSULE, DELAYED REL PELLETS;ORAL - 500MG;500MG;30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
                    • FOR SUSPENSION;ORAL - 200MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
                    • FOR SUSPENSION;ORAL - 400MG/5ML
                    • TABLET, EXTENDED RELEASE;ORAL - 1GM;EQ 62.5MG BASE
                    • TABLET, EXTENDED RELEASE;ORAL - 775MG
                    • CAPSULE, TABLET, CAPSULE, DELAYED RELEASE;ORAL - 500MG,N/A,N/A;N/A,500MG,N/A;N/A,N/A,20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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                    famar-2024-07-22

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