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    NDC 63629-8236-01 Ranitidine 150 mg/1 Details

    Ranitidine 150 mg/1

    Ranitidine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is RANITIDINE HYDROCHLORIDE.

    Product Information

    NDC 63629-8236
    Product ID 63629-8236_dd505d62-58c5-4f3b-aa28-a75e71913ab0
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Ranitidine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ranitidine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 150
    Active Ingredient Units mg/1
    Substance Name RANITIDINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077824
    Listing Certified Through 2023-12-31

    Package

    NDC 63629-8236-01 (63629823601)

    NDC Package Code 63629-8236-1
    Billing NDC 63629823601
    Package 30 TABLET in 1 BOTTLE (63629-8236-1)
    Marketing Start Date 2021-12-23
    NDC Exclude Flag N
    Pricing Information N/A
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