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    NDC 53002-1579-03 Citalopram Hydrobromide 10 mg/1 Details

    Citalopram Hydrobromide 10 mg/1

    Citalopram Hydrobromide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RPK Pharmaceuticals, Inc.. The primary component is CITALOPRAM HYDROBROMIDE.

    Product Information

    NDC 53002-1579
    Product ID 53002-1579_42dfeb78-bce9-43b2-9d5c-d71f03e11653
    Associated GPIs 58160020100310
    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 Citalopram Hydrobromide
    Proprietary Name Suffix n/a
    Non-Proprietary Name Citalopram Hydrobromide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name CITALOPRAM HYDROBROMIDE
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078216
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1579-03 (53002157903)

    NDC Package Code 53002-1579-3
    Billing NDC 53002157903
    Package 30 TABLET in 1 BOTTLE (53002-1579-3)
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A