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    Approved Drug Products containing 75416 listed in the FDA Orange Book. Original Data : FDA Website

    EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

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    Bora Pharmaceuticals- Making success more certain.

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    Polfa Tarchomin is a leading Polish pharmaceutical company with 200 year tradition in manufacture and sale of pharmaceutical products.

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    Minakem offers CDMO services for API & HPAPI, generics, regulatory expertise, track record performance & FDA & GMP certifications.

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    Axplora- The partner of choice for complex APIs.

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    Fareva is a one-stop-shop for API/HPAPI, OSD & Sterile products, is USFDA, EMA and PMDA-inspected and has multiple NDA & ANDA filings.

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    Actavis Inc

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    Brand Name : NAPROXEN SODIUM

    Ireland
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    Not Confirmed
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    Brand Name : NAPROXEN SODIUM

    Ireland
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    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

    NAPROXEN SODIUM

    Actavis Inc

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : NAPROXEN SODIUM

    Dosage Strength : EQ 375MG BASE

    Approval Date : 2003-04-23

    Application Number : 75416

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : NAPROXEN SODIUM

    Ireland
    Luxepack
    Not Confirmed
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    Brand Name : NAPROXEN SODIUM

    Ireland
    Luxepack
    Not Confirmed
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    • 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

    NAPROXEN SODIUM

    Actavis Inc

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : NAPROXEN SODIUM

    Dosage Strength : EQ 750MG BASE

    Approval Date : 2016-08-11

    Application Number : 75416

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    03

    Brand Name : NAPROXEN SODIUM

    Ireland
    Luxepack
    Not Confirmed
    arrow

    Brand Name : NAPROXEN SODIUM

    Ireland
    Luxepack
    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 Ireland
    Virtual Booth Virtual Booth
    Digital Content Digital Content

    RLD : No

    TE Code : AB

    NAPROXEN SODIUM

    Actavis Inc

    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : NAPROXEN SODIUM

    Dosage Strength : EQ 500MG BASE

    Approval Date : 2002-08-27

    Application Number : 75416

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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