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    NDC 70518-1917-00 Citalopram Hydrobromide 20 mg/1 Details

    Citalopram Hydrobromide 20 mg/1

    Citalopram Hydrobromide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is CITALOPRAM HYDROBROMIDE.

    Product Information

    NDC 70518-1917
    Product ID 70518-1917_0ac1f742-681e-f508-e063-6294a90a964b
    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 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 20
    Active Ingredient Units mg/1
    Substance Name CITALOPRAM HYDROBROMIDE
    Labeler Name REMEDYREPACK 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 70518-1917-00 (70518191700)

    NDC Package Code 70518-1917-0
    Billing NDC 70518191700
    Package 30 TABLET in 1 BLISTER PACK (70518-1917-0)
    Marketing Start Date 2019-02-27
    NDC Exclude Flag N
    Pricing Information N/A