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    NDC 70518-2597-00 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 REMEDYREPACK INC.. The primary component is ESCITALOPRAM OXALATE.

    Product Information

    NDC 70518-2597
    Product ID 70518-2597_05cd7548-4b2c-da5b-e063-6394a90a4b3b
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Escitalopram
    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 REMEDYREPACK INC.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078032
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2597-00 (70518259700)

    NDC Package Code 70518-2597-0
    Billing NDC 70518259700
    Package 100 POUCH in 1 BOX (70518-2597-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2597-1)
    Marketing Start Date 2020-02-25
    NDC Exclude Flag N
    Pricing Information N/A