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    NDC 68788-7169-01 Eszopiclone 3 mg/1 Details

    Eszopiclone 3 mg/1

    Eszopiclone 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 ESZOPICLONE.

    Product Information

    NDC 68788-7169
    Product ID 68788-7169_9c5a33e7-778f-4ab2-b2c0-3bdfc08dc624
    Associated GPIs 60204035000340
    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 Eszopiclone
    Proprietary Name Suffix n/a
    Non-Proprietary Name Eszopiclone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 3
    Active Ingredient Units mg/1
    Substance Name ESZOPICLONE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class n/a
    DEA Schedule CIV
    Marketing Category ANDA
    Application Number ANDA202929
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7169-01 (68788716901)

    NDC Package Code 68788-7169-1
    Billing NDC 68788716901
    Package 10 TABLET, FILM COATED in 1 BOTTLE (68788-7169-1)
    Marketing Start Date 2018-06-11
    NDC Exclude Flag N
    Pricing Information N/A