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    NDC 71335-1307-03 Escitalopram 20 mg/1 Details

    Escitalopram 20 mg/1

    Escitalopram is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is ESCITALOPRAM OXALATE.

    Product Information

    NDC 71335-1307
    Product ID 71335-1307_8f8cfa7f-ced5-4f33-8ceb-3d4027b4e6e9
    Associated GPIs 58160034100330
    GCN Sequence Number 050760
    GCN Sequence Number Description escitalopram oxalate TABLET 20 MG ORAL
    HIC3 H2S
    HIC3 Description SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
    GCN 17987
    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
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name ESCITALOPRAM OXALATE
    Labeler Name Bryant Ranch Prepack
    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 71335-1307-03 (71335130703)

    NDC Package Code 71335-1307-3
    Billing NDC 71335130703
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71335-1307-3)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A