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    NDC 76420-0628-01 Ramelteon 8 mg/1 Details

    Ramelteon 8 mg/1

    Ramelteon is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Asclemed USA, Inc.. The primary component is RAMELTEON.

    Product Information

    NDC 76420-0628
    Product ID 76420-628_0b2fcb56-d9fa-e9f6-e063-6294a90a2f8e
    Associated GPIs
    GCN Sequence Number 059509
    GCN Sequence Number Description ramelteon TABLET 8 MG ORAL
    HIC3 H8B
    HIC3 Description HYPNOTICS, MELATONIN MT1/MT2 RECEPTOR AGONISTS
    GCN 25202
    HICL Sequence Number 033126
    HICL Sequence Number Description RAMELTEON
    Brand/Generic Generic
    Proprietary Name Ramelteon
    Proprietary Name Suffix n/a
    Non-Proprietary Name Ramelteon
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 8
    Active Ingredient Units mg/1
    Substance Name RAMELTEON
    Labeler Name Asclemed USA, Inc.
    Pharmaceutical Class Melatonin Receptor Agonist [EPC], Melatonin Receptor Agonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211567
    Listing Certified Through 2024-12-31

    Package

    NDC 76420-0628-01 (76420062801)

    NDC Package Code 76420-628-01
    Billing NDC 76420062801
    Package 100 TABLET in 1 BOTTLE (76420-628-01)
    Marketing Start Date 2023-10-17
    NDC Exclude Flag N
    Pricing Information N/A