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    NDC 71335-0830-02 Lamotrigine 200 mg/1 Details

    Lamotrigine 200 mg/1

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

    Product Information

    NDC 71335-0830
    Product ID 71335-0830_cbf3ec29-66dd-4a92-a951-53a21a3e1c44
    Associated GPIs 72600040000340
    GCN Sequence Number 022551
    GCN Sequence Number Description lamotrigine TABLET 200 MG ORAL
    HIC3 H4B
    HIC3 Description ANTICONVULSANTS
    GCN 64325
    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
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name LAMOTRIGINE
    Labeler Name Bryant Ranch Prepack
    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 ANDA090170
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0830-02 (71335083002)

    NDC Package Code 71335-0830-2
    Billing NDC 71335083002
    Package 60 TABLET in 1 BOTTLE (71335-0830-2)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A