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    NDC 70518-1291-00 escitalopram oxalate 5 mg/1 Details

    escitalopram oxalate 5 mg/1

    escitalopram oxalate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is ESCITALOPRAM OXALATE.

    Product Information

    NDC 70518-1291
    Product ID 70518-1291_e3b3fd2c-7eae-2048-e053-2a95a90a3572
    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
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name ESCITALOPRAM OXALATE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090939
    Listing Certified Through 2023-12-31

    Package

    NDC 70518-1291-00 (70518129100)

    NDC Package Code 70518-1291-0
    Billing NDC 70518129100
    Package 30 TABLET in 1 BLISTER PACK (70518-1291-0)
    Marketing Start Date 2018-07-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 02689e49-25ac-4116-a649-6825e6000ff6 Details

    Revised: 7/2022