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    NDC 69097-0823-02 Citalopram 20 mg/1 Details

    Citalopram 20 mg/1

    Citalopram is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cipla USA Inc.. The primary component is CITALOPRAM HYDROBROMIDE.

    Product Information

    NDC 69097-0823
    Product ID 69097-823_f6e72240-0d92-418a-b6d2-9658e8caf652
    Associated GPIs 58160020100320
    GCN Sequence Number 046203
    GCN Sequence Number Description citalopram hydrobromide TABLET 20 MG ORAL
    HIC3 H2S
    HIC3 Description SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
    GCN 16342
    HICL Sequence Number 010321
    HICL Sequence Number Description CITALOPRAM HYDROBROMIDE
    Brand/Generic Generic
    Proprietary Name Citalopram
    Proprietary Name Suffix n/a
    Non-Proprietary Name Citalopram
    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 Cipla USA Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077534
    Listing Certified Through 2024-12-31

    Package

    NDC 69097-0823-02 (69097082302)

    NDC Package Code 69097-823-02
    Billing NDC 69097082302
    Package 30 TABLET in 1 BOTTLE (69097-823-02)
    Marketing Start Date 2016-07-22
    NDC Exclude Flag N
    Pricing Information N/A