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    NDC 62856-0455-10 DAYVIGO 5 mg/1 Details

    DAYVIGO 5 mg/1

    DAYVIGO is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Eisai Inc.. The primary component is LEMBOREXANT.

    Product Information

    NDC 62856-0455
    Product ID 62856-455_c4274f49-6deb-4d9a-bd64-21728c025394
    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 DAYVIGO
    Proprietary Name Suffix n/a
    Non-Proprietary Name lemborexant
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name LEMBOREXANT
    Labeler Name Eisai Inc.
    Pharmaceutical Class Cytochrome P450 2B6 Inducers [MoA], Orexin Receptor Antagonist [EPC], Orexin Receptor Antagonists [MoA]
    DEA Schedule CIV
    Marketing Category NDA
    Application Number NDA212028
    Listing Certified Through 2023-12-31

    Package

    NDC 62856-0455-10 (62856045510)

    NDC Package Code 62856-455-10
    Billing NDC 62856045510
    Package 5 CARTON in 1 TRAY (62856-455-10) / 1 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2020-04-07
    NDC Exclude Flag N
    Pricing Information N/A