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    NDC 62856-0410-90 DAYVIGO 10 mg/1 Details

    DAYVIGO 10 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 62856-0410
    Product ID 62856-410_e183487a-05cb-44e3-ba3d-858b29efb563
    Associated GPIs 60500040000340
    GCN Sequence Number 080591
    GCN Sequence Number Description lemborexant TABLET 10 MG ORAL
    HIC3 H2E
    HIC3 Description SEDATIVE-HYPNOTICS,NON-BARBITURATE
    GCN 47484
    HICL Sequence Number 046275
    HICL Sequence Number Description LEMBOREXANT
    Brand/Generic Brand
    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 10
    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 2024-12-31

    Package

    NDC 62856-0410-90 (62856041090)

    NDC Package Code 62856-410-90
    Billing NDC 62856041090
    Package 90 TABLET, FILM COATED in 1 BOTTLE (62856-410-90)
    Marketing Start Date 2020-04-07
    NDC Exclude Flag N
    Pricing Information N/A