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    Brand Name : UROCIT-K

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    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : UROCIT-K

    Dosage Strength : 5MEQ

    Approval Date : 1985-08-30

    Application Number : 19071

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    POTASSIUM CITRATE

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    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : UROCIT-K

    Dosage Strength : 10MEQ

    Approval Date : 1992-08-31

    Application Number : 19071

    RX/OTC/DISCN : RX

    RLD : Yes

    TE Code : AB

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    Brand Name : UROCIT-K

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    POTASSIUM CITRATE

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    Dosage Form : TABLET, EXTENDED RELEASE; ORAL

    Proprietary Name : UROCIT-K

    Dosage Strength : 15MEQ

    Approval Date : 2009-12-30

    Application Number : 19071

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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.