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    NDC 68788-7559-09 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 Preferred Pharmaceuticals, Inc.. The primary component is ESCITALOPRAM OXALATE.

    Product Information

    NDC 68788-7559
    Product ID 68788-7559_ddce18c6-ab27-4f2e-a5e3-65b213b9bb95
    Associated GPIs 58160034100310
    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 Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078032
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7559-09 (68788755909)

    NDC Package Code 68788-7559-9
    Billing NDC 68788755909
    Package 90 TABLET, FILM COATED in 1 BOTTLE (68788-7559-9)
    Marketing Start Date 2019-12-27
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b23d737b-8718-46f1-b2cf-06136a98aa68 Details

    Revised: 5/2022