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    NDC 67877-0555-10 Dimethyl fumarate 120 mg/1 Details

    Dimethyl fumarate 120 mg/1

    Dimethyl fumarate is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is DIMETHYL FUMARATE.

    Product Information

    NDC 67877-0555
    Product ID 67877-555_a9067e3a-ce17-41ee-9a31-844e838ffc1f
    Associated GPIs 62405525006520
    GCN Sequence Number 070786
    GCN Sequence Number Description dimethyl fumarate CAPSULE DR 120 MG ORAL
    HIC3 H0E
    HIC3 Description AGENTS TO TREAT MULTIPLE SCLEROSIS
    GCN 34434
    HICL Sequence Number 040168
    HICL Sequence Number Description DIMETHYL FUMARATE
    Brand/Generic Generic
    Proprietary Name Dimethyl fumarate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dimethyl fumarate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 120
    Active Ingredient Units mg/1
    Substance Name DIMETHYL FUMARATE
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA210440
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0555-10 (67877055510)

    NDC Package Code 67877-555-10
    Billing NDC 67877055510
    Package 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67877-555-10)
    Marketing Start Date 2020-09-26
    NDC Exclude Flag N
    Pricing Information N/A