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    NDC 53746-0020-10 Escitalopram Oxalate 10 mg/1 Details

    Escitalopram Oxalate 10 mg/1

    Escitalopram Oxalate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals of New York LLC. The primary component is ESCITALOPRAM OXALATE.

    Product Information

    NDC 53746-0020
    Product ID 53746-020_4c0cc309-a167-412b-90af-d88b28d5ea0e
    Associated GPIs
    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 Escitalopram Oxalate
    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 10
    Active Ingredient Units mg/1
    Substance Name ESCITALOPRAM OXALATE
    Labeler Name Amneal Pharmaceuticals of New York LLC
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205619
    Listing Certified Through 2024-12-31

    Package

    NDC 53746-0020-10 (53746002010)

    NDC Package Code 53746-020-10
    Billing NDC 53746002010
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (53746-020-10)
    Marketing Start Date 2017-05-17
    NDC Exclude Flag N
    Pricing Information N/A