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    NDC 42291-0443-30 Lamotrigine 25 mg/1 Details

    Lamotrigine 25 mg/1

    Lamotrigine is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is LAMOTRIGINE.

    Product Information

    NDC 42291-0443
    Product ID 42291-443_0e8fa652-212f-4339-e063-6294a90abce6
    Associated GPIs 72600040007510
    GCN Sequence Number 065250
    GCN Sequence Number Description lamotrigine TAB ER 24 25 MG ORAL
    HIC3 H4B
    HIC3 Description ANTICONVULSANTS
    GCN 24693
    HICL Sequence Number 007378
    HICL Sequence Number Description LAMOTRIGINE
    Brand/Generic Generic
    Proprietary Name Lamotrigine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lamotrigine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name LAMOTRIGINE
    Labeler Name AvKARE
    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 ANDA207497
    Listing Certified Through 2025-12-31

    Package

    NDC 42291-0443-30 (42291044330)

    NDC Package Code 42291-443-30
    Billing NDC 42291044330
    Package 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-443-30)
    Marketing Start Date 2020-05-22
    NDC Exclude Flag N
    Pricing Information N/A