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    Sodium Carbonate Monohydrate

    ACTIVE PHARMA INGREDIENTS

    FINISHED DOSAGE FORMULATIONS

    MARKET PLACE

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    01 1B. Braun Medizintechnologie Gmbh

    02 1Nordic Drugs Ab

    03 9Teva Pharma Slu

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    01

    B. Braun Medizintechnologie Gmbh

    Germany
    FNCE
    Not Confirmed
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    B. Braun Medizintechnologie Gmbh

    Germany
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    FNCE
    Not Confirmed
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Sodium Chloride Sodium Bicarbonate

    Brand Name : Bicaflac Buffer

    Dosage Form : Dialysis Solution

    Dosage Strength :

    Packaging :

    Approval Date : 19/10/2001

    Application Number : 20011019000077

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    02

    Nordic Drugs Ab

    Sweden
    FNCE
    Not Confirmed
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    Nordic Drugs Ab

    Sweden
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    FNCE
    Not Confirmed
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    Regulatory Info : Approved

    Registration Country : Sweden

    Alginic Acid Alumina; Alginic Acid Alumina; Hydrated Sodium Bicarbonate

    Brand Name : Gaviscon

    Dosage Form : Chewable Tablet

    Dosage Strength :

    Packaging :

    Approval Date : 30/08/1974

    Application Number : 19740830000013

    Regulatory Info : Approved

    Registration Country : Sweden

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    03

    Teva Pharma Slu

    Israel
    FNCE
    Not Confirmed
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    Teva Pharma Slu

    Israel
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    FNCE
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    Regulatory Info : Authorized

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Alendronic Acid/Colecalciferol Tevagen

    Dosage Form : Tablet

    Dosage Strength : 70MG; 5,600 IU

    Packaging :

    Approval Date : 2014-11-13

    Application Number : 78795

    Regulatory Info : Authorized

    Registration Country : Spain

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    04

    Teva Pharma Slu

    Israel
    FNCE
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    Teva Pharma Slu

    Israel
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    FNCE
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Acido Alendronico/Colecalciferol Semanal Ratio

    Dosage Form : Tablet

    Dosage Strength : 70MG; 2,800 IU

    Packaging :

    Approval Date : 2019-12-11

    Application Number : 81502

    Regulatory Info : Cancelled

    Registration Country : Spain

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    05

    Teva Pharma Slu

    Israel
    FNCE
    Not Confirmed
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    Teva Pharma Slu

    Israel
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    FNCE
    Not Confirmed
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    Regulatory Info : Authorized

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Alendronic Acid/Colecalciferol Tevagen

    Dosage Form : Tablet

    Dosage Strength : 70MG; 2,800 IU

    Packaging :

    Approval Date : 2014-11-13

    Application Number : 78794

    Regulatory Info : Authorized

    Registration Country : Spain

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    06

    Teva Pharma Slu

    Israel
    FNCE
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    Teva Pharma Slu

    Israel
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    FNCE
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    Regulatory Info : Authorized

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Alendronic Acid/Colecalciferol Ratiopharm

    Dosage Form : Tablet

    Dosage Strength : 70MG; 2,800 IU

    Packaging :

    Approval Date : 2014-11-13

    Application Number : 78796

    Regulatory Info : Authorized

    Registration Country : Spain

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    07

    Teva Pharma Slu

    Israel
    FNCE
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    Teva Pharma Slu

    Israel
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    FNCE
    Not Confirmed
    • fda
    • EDQM
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    Flag Israel
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Alendronic Acid/Cholecalciferol Weekly Teva

    Dosage Form : Tablet

    Dosage Strength : 70MG; 2,800 IU

    Packaging :

    Approval Date : 2019-12-05

    Application Number : 81501

    Regulatory Info : Cancelled

    Registration Country : Spain

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    08

    Teva Pharma Slu

    Israel
    FNCE
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    Teva Pharma Slu

    Israel
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    FNCE
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Acido Alendronico/Colecalciferol Semanal Ratio

    Dosage Form : Tablet

    Dosage Strength : 70MG; 5,600 IU

    Packaging :

    Approval Date : 2019-12-11

    Application Number : 81503

    Regulatory Info : Cancelled

    Registration Country : Spain

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    09

    Teva Pharma Slu

    Israel
    FNCE
    Not Confirmed
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    Teva Pharma Slu

    Israel
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    FNCE
    Not Confirmed
    • fda
    • EDQM
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    Flag Israel
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    Regulatory Info : Cancelled

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Alendronic Acid/Cholecalciferol Weekly Teva

    Dosage Form : Tablet

    Dosage Strength : 70MG; 5,600 IU

    Packaging :

    Approval Date : 2019-12-11

    Application Number : 81500

    Regulatory Info : Cancelled

    Registration Country : Spain

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    10

    Teva Pharma Slu

    Israel
    FNCE
    Not Confirmed
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    Teva Pharma Slu

    Israel
    arrow
    FNCE
    Not Confirmed
    • fda
    • EDQM
    • WHO-GMP
    Virtual Booth Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass. Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
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    Flag Israel
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    Regulatory Info : Authorized

    Registration Country : Spain

    Cholecalciferol; Alendronate Sodium Monohydrate

    Brand Name : Alendronic Acid/Colecalciferol Ratiopharm

    Dosage Form : Tablet

    Dosage Strength : 70MG; 5,600 IU

    Packaging :

    Approval Date : 2014-11-13

    Application Number : 78797

    Regulatory Info : Authorized

    Registration Country : Spain

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