Search by Drug Name or NDC

    NDC 70518-2563-01 Lamotrigine 100 mg/1 Details

    Lamotrigine 100 mg/1

    Lamotrigine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is LAMOTRIGINE.

    Product Information

    NDC 70518-2563
    Product ID 70518-2563_0b62b660-87b2-88a7-e063-6294a90a3d26
    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 100
    Active Ingredient Units mg/1
    Substance Name LAMOTRIGINE
    Labeler Name REMEDYREPACK 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 70518-2563-01 (70518256301)

    NDC Package Code 70518-2563-1
    Billing NDC 70518256301
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70518-2563-1)
    Marketing Start Date 2022-11-10
    NDC Exclude Flag N
    Pricing Information N/A