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    NDC 64406-0020-03 Vumerity 231 mg/1 Details

    Vumerity 231 mg/1

    Vumerity is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Biogen Inc.. The primary component is DIROXIMEL FUMARATE.

    Product Information

    NDC 64406-0020
    Product ID 64406-020_c77c2a1a-cfb5-4c6e-ac79-4cfa8f3109e2
    Associated GPIs 62405530006520 62405530006540
    GCN Sequence Number 080393
    GCN Sequence Number Description diroximel fumarate CAPSULE DR 231 MG ORAL
    HIC3 H0E
    HIC3 Description AGENTS TO TREAT MULTIPLE SCLEROSIS
    GCN 47209
    HICL Sequence Number 046164
    HICL Sequence Number Description DIROXIMEL FUMARATE
    Brand/Generic Brand
    Proprietary Name Vumerity
    Proprietary Name Suffix n/a
    Non-Proprietary Name diroximel fumarate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 231
    Active Ingredient Units mg/1
    Substance Name DIROXIMEL FUMARATE
    Labeler Name Biogen Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA211855
    Listing Certified Through 2025-12-31

    Package

    NDC 64406-0020-03 (64406002003)

    NDC Package Code 64406-020-03
    Billing NDC 64406002003
    Package 1 BOTTLE, PLASTIC in 1 CARTON (64406-020-03) / 120 CAPSULE in 1 BOTTLE, PLASTIC
    Marketing Start Date 2019-10-29
    NDC Exclude Flag N
    Pricing Information N/A