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    NDC 68788-8962-01 Citalopram Hydrobromide 40 mg/1 Details

    Citalopram Hydrobromide 40 mg/1

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

    Product Information

    NDC 68788-8962
    Product ID 68788-8962_88bd9f99-7dcd-40a2-9591-4aac5cd82645
    Associated GPIs 58160020100340
    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 40
    Active Ingredient Units mg/1
    Substance Name CITALOPRAM HYDROBROMIDE
    Labeler Name Preferred 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 68788-8962-01 (68788896201)

    NDC Package Code 68788-8962-1
    Billing NDC 68788896201
    Package 100 TABLET in 1 BOTTLE (68788-8962-1)
    Marketing Start Date 2016-01-04
    NDC Exclude Flag N
    Pricing Information N/A