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    NDC 68382-0011-05 Lamotrigine 250 mg/1 Details

    Lamotrigine 250 mg/1

    Lamotrigine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is LAMOTRIGINE.

    Product Information

    NDC 68382-0011
    Product ID 68382-011_6ab4eff7-1c04-465f-a752-63149bca1d36
    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 Lamotrigine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lamotrigine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 250
    Active Ingredient Units mg/1
    Substance Name LAMOTRIGINE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Anti-epileptic Agent [EPC], Decreased Central Nervous System Disorganized Electrical Activity [PE], Dihydrofolate Reductase Inhibitors [MoA], Mood Stabilizer [EPC], Organic Cation Transporter 2 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077633
    Listing Certified Through 2024-12-31

    Package

    NDC 68382-0011-05 (68382001105)

    NDC Package Code 68382-011-05
    Billing NDC 68382001105
    Package 500 TABLET in 1 BOTTLE (68382-011-05)
    Marketing Start Date 2009-01-27
    NDC Exclude Flag N
    Pricing Information N/A