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    NDC 71205-0168-30 Escitalopram 10 mg/1 Details

    Escitalopram 10 mg/1

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

    Product Information

    NDC 71205-0168
    Product ID 71205-168_bfd7c6f5-24c7-4491-b4f8-d501a2393fec
    Associated GPIs 58160034100320
    GCN Sequence Number 050712
    GCN Sequence Number Description escitalopram oxalate TABLET 10 MG ORAL
    HIC3 H2S
    HIC3 Description SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
    GCN 17851
    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 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 Proficient Rx LP
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090432
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0168-30 (71205016830)

    NDC Package Code 71205-168-30
    Billing NDC 71205016830
    Package 30 TABLET, FILM COATED in 1 BOTTLE (71205-168-30)
    Marketing Start Date 2012-09-11
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 2d0b4839-e4d1-4e0e-9dc0-ba821f266472 Details

    Revised: 4/2022