Search by Drug Name or NDC

    NDC 53002-1360-00 Citalopram 40 mg/1 Details

    Citalopram 40 mg/1

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

    Product Information

    NDC 53002-1360
    Product ID 53002-1360_3cbfb31c-3e52-40b5-8aef-2ea42f73a242
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Citalopram Hydrobromide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 40
    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 ANDA077031
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1360-00 (53002136000)

    NDC Package Code 53002-1360-0
    Billing NDC 53002136000
    Package 100 TABLET, FILM COATED in 1 BOTTLE (53002-1360-0)
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A