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    Brand Name : CEFUROXIME AXETIL

    India
    India Med Expo
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    Brand Name : CEFUROXIME AXETIL

    India
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    RLD : No

    TE Code : AB

    CEFUROXIME AXETIL

    Aurobindo Pharma Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFUROXIME AXETIL

    Dosage Strength : EQ 500MG BASE

    Approval Date : 2006-03-29

    Application Number : 65308

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : CEFUROXIME AXETIL

    India
    India Med Expo
    Not Confirmed
    arrow

    Brand Name : CEFUROXIME AXETIL

    India
    India Med Expo
    Not Confirmed
    arrow
    • 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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    RLD : No

    TE Code : AB

    CEFUROXIME AXETIL

    Aurobindo Pharma Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFUROXIME AXETIL

    Dosage Strength : EQ 125MG BASE

    Approval Date : 2006-03-29

    Application Number : 65308

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Stock Recap
    #PipelineProspector

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    03

    Brand Name : CEFUROXIME AXETIL

    India
    India Med Expo
    Not Confirmed
    arrow

    Brand Name : CEFUROXIME AXETIL

    India
    India Med Expo
    Not Confirmed
    arrow
    • 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.
    Post an Enquiry Post an Enquiry
    Flag India
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code : AB

    CEFUROXIME AXETIL

    Aurobindo Pharma Limited

    Dosage Form : TABLET; ORAL

    Proprietary Name : CEFUROXIME AXETIL

    Dosage Strength : EQ 250MG BASE

    Approval Date : 2006-03-29

    Application Number : 65308

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

    blank

    Product
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    Stock Recap
    #PipelineProspector

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