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    NDC 65162-0664-90 Ranitidine 15 mg/mL Details

    Ranitidine 15 mg/mL

    Ranitidine is a ORAL SOLUTION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals LLC. The primary component is RANITIDINE HYDROCHLORIDE.

    Product Information

    NDC 65162-0664
    Product ID 65162-664_917462a4-6f47-4e77-8961-ccdb02412647
    Associated GPIs 49200020101210
    GCN Sequence Number 011672
    GCN Sequence Number Description ranitidine HCl SYRUP 15 MG/ML ORAL
    HIC3 Z2D
    HIC3 Description HISTAMINE H2-RECEPTOR INHIBITORS
    GCN 12090
    HICL Sequence Number 004520
    HICL Sequence Number Description RANITIDINE HCL
    Brand/Generic Generic
    Proprietary Name Ranitidine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ranitidine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 15
    Active Ingredient Units mg/mL
    Substance Name RANITIDINE HYDROCHLORIDE
    Labeler Name Amneal Pharmaceuticals LLC
    Pharmaceutical Class Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078312
    Listing Certified Through 2023-12-31

    Package

    NDC 65162-0664-90 (65162066490)

    NDC Package Code 65162-664-90
    Billing NDC 65162066490
    Package 473 mL in 1 BOTTLE (65162-664-90)
    Marketing Start Date 2010-03-12
    NDC Exclude Flag N
    Pricing Information N/A