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    Approved Drug Products containing 19090 listed in the FDA Orange Book. Original Data : FDA Website

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    PAI Pharmaceutical Associates

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    Brand Name : ZANTAC

    U.S.A
    AAPS 2024
    Not Confirmed
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    Brand Name : ZANTAC

    U.S.A
    AAPS 2024
    Not Confirmed
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    RLD : Yes

    TE Code :

    RANITIDINE HYDROCHLORIDE

    PAI Pharmaceutical Associates

    Dosage Form : INJECTABLE; INJECTION

    Proprietary Name : ZANTAC

    Dosage Strength : EQ 25MG BASE/ML

    Approval Date : 1984-10-19

    Application Number : 19090

    RX/OTC/DISCN : DISCN

    RLD : Yes

    TE Code :

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