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    Brand Name : SUCRALFATE

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    RLD : No

    TE Code : AB

    SUCRALFATE

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    Dosage Form : SUSPENSION; ORAL

    Proprietary Name : SUCRALFATE

    Dosage Strength : 1GM/10ML

    Approval Date : 2024-05-21

    Application Number : 216474

    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.