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    NDC 68180-0802-06 RUFINAMIDE 100 mg/1 Details

    RUFINAMIDE 100 mg/1

    RUFINAMIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals, Inc.. The primary component is RUFINAMIDE.

    Product Information

    NDC 68180-0802
    Product ID 68180-802_29588ca0-0dde-4a46-be19-0e58db8baa49
    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 RUFINAMIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name rufinamide
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name RUFINAMIDE
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204964
    Listing Certified Through 2023-12-31

    Package

    NDC 68180-0802-06 (68180080206)

    NDC Package Code 68180-802-06
    Billing NDC 68180080206
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68180-802-06)
    Marketing Start Date 2022-11-28
    NDC Exclude Flag N
    Pricing Information N/A
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