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    NDC 70518-1827-00 Levetiracetam 750 mg/1 Details

    Levetiracetam 750 mg/1

    Levetiracetam is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is LEVETIRACETAM.

    Product Information

    NDC 70518-1827
    Product ID 70518-1827_0aaf392b-0d27-de6f-e063-6294a90a539b
    Associated GPIs
    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 Levetiracetam
    Proprietary Name Suffix n/a
    Non-Proprietary Name Levetiracetam
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name LEVETIRACETAM
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Decreased Central Nervous System Disorganized Electrical Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078154
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1827-00 (70518182700)

    NDC Package Code 70518-1827-0
    Billing NDC 70518182700
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1827-0)
    Marketing Start Date 2019-01-26
    NDC Exclude Flag N
    Pricing Information N/A