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    NDC 68180-0137-06 Escitalopram 5 mg/1 Details

    Escitalopram 5 mg/1

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

    Product Information

    NDC 68180-0137
    Product ID 68180-137_a752cb19-7de3-4b6d-aa44-03b7027ea60b
    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 Escitslopram
    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 Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078169
    Listing Certified Through 2024-12-31

    Package

    NDC 68180-0137-06 (68180013706)

    NDC Package Code 68180-137-06
    Billing NDC 68180013706
    Package 30 TABLET in 1 BOTTLE (68180-137-06)
    Marketing Start Date 2012-09-10
    NDC Exclude Flag N
    Pricing Information N/A