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    NDC 00456-4020-63 Celexa 20 mg/1 Details

    Celexa 20 mg/1

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

    Product Information

    NDC 00456-4020
    Product ID 0456-4020_a6e5794d-438d-4fb9-8303-6a57d7b64da6
    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 Brand
    Proprietary Name Celexa
    Proprietary Name Suffix n/a
    Non-Proprietary Name citalopram
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name CITALOPRAM HYDROBROMIDE
    Labeler Name Allergan, Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020822
    Listing Certified Through 2024-12-31

    Package

    NDC 00456-4020-63 (00456402063)

    NDC Package Code 0456-4020-63
    Billing NDC 00456402063
    Package 10 BLISTER PACK in 1 BOX, UNIT-DOSE (0456-4020-63) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0456-4020-11)
    Marketing Start Date 1998-07-17
    NDC Exclude Flag N
    Pricing Information N/A