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    NDC 69102-0106-01 Levetiracetam 750 mg/1 Details

    Levetiracetam 750 mg/1

    Levetiracetam is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by OWP Pharmaceuticals, Inc.. The primary component is LEVETIRACETAM.

    Product Information

    NDC 69102-0106
    Product ID 69102-106_14899d4b-b295-431e-b1d5-d8163bdadb87
    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
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name LEVETIRACETAM
    Labeler Name OWP Pharmaceuticals, Inc.
    Pharmaceutical Class Decreased Central Nervous System Disorganized Electrical Activity [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078858
    Listing Certified Through 2024-12-31

    Package

    NDC 69102-0106-01 (69102010601)

    NDC Package Code 69102-106-01
    Billing NDC 69102010601
    Package 120 TABLET in 1 BOTTLE (69102-106-01)
    Marketing Start Date 2020-10-28
    NDC Exclude Flag N
    Pricing Information N/A
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