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    NDC 59746-0279-30 Escitalopram 5 mg/1 Details

    Escitalopram 5 mg/1

    Escitalopram is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Jubilant Cadista Pharmaceuticals Inc.. The primary component is ESCITALOPRAM OXALATE.

    Product Information

    NDC 59746-0279
    Product ID 59746-279_bd1bbdbe-e0cf-48d5-9526-b3f4c330be7e
    Associated GPIs 58160034100310
    GCN Sequence Number 051642
    GCN Sequence Number Description escitalopram oxalate TABLET 5 MG ORAL
    HIC3 H2S
    HIC3 Description SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
    GCN 18975
    HICL Sequence Number 024022
    HICL Sequence Number Description ESCITALOPRAM OXALATE
    Brand/Generic Generic
    Proprietary Name Escitalopram
    Proprietary Name Suffix n/a
    Non-Proprietary Name Escitalopram Oxalate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name ESCITALOPRAM OXALATE
    Labeler Name Jubilant Cadista Pharmaceuticals Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202280
    Listing Certified Through 2024-12-31

    Package

    NDC 59746-0279-30 (59746027930)

    NDC Package Code 59746-279-30
    Billing NDC 59746027930
    Package 30 TABLET, FILM COATED in 1 BOTTLE (59746-279-30)
    Marketing Start Date 2024-01-01
    NDC Exclude Flag N
    Pricing Information N/A