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    Brand Name : NAPROXEN

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    RLD : No

    TE Code : AB

    NAPROXEN

    Zydus Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROXEN

    Dosage Strength : 375MG

    Approval Date : 2007-06-07

    Application Number : 78620

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : NAPROXEN

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    RLD : No

    TE Code : AB

    NAPROXEN

    Zydus Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROXEN

    Dosage Strength : 500MG

    Approval Date : 2007-06-07

    Application Number : 78620

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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    Brand Name : NAPROXEN

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    BePharma
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    Brand Name : NAPROXEN

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    • EDQM
    • WHO-GMP
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    RLD : No

    TE Code : AB

    NAPROXEN

    Zydus Pharmaceuticals

    Dosage Form : TABLET; ORAL

    Proprietary Name : NAPROXEN

    Dosage Strength : 250MG

    Approval Date : 2007-06-07

    Application Number : 78620

    RX/OTC/DISCN : RX

    RLD : No

    TE Code : AB

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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.