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    NDC 57841-1301-04 MOVANTIK 25 mg/1 Details

    MOVANTIK 25 mg/1

    MOVANTIK is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by RedHill Biopharma Ltd. The primary component is NALOXEGOL OXALATE.

    Product Information

    NDC 57841-1301
    Product ID 57841-1301_3da484be-32a1-4265-b58e-fa55b7acd59a
    Associated GPIs 52580060300330
    GCN Sequence Number 073336
    GCN Sequence Number Description naloxegol oxalate TABLET 25 MG ORAL
    HIC3 H3Y
    HIC3 Description MU-OPIOID RECEPTOR ANTAGONISTS,PERIPHERALLY-ACTING
    GCN 37726
    HICL Sequence Number 041686
    HICL Sequence Number Description NALOXEGOL OXALATE
    Brand/Generic Brand
    Proprietary Name MOVANTIK
    Proprietary Name Suffix n/a
    Non-Proprietary Name naloxegol oxalate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name NALOXEGOL OXALATE
    Labeler Name RedHill Biopharma Ltd
    Pharmaceutical Class Opioid Antagonist [EPC], Opioid Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA204760
    Listing Certified Through 2024-12-31

    Package

    NDC 57841-1301-04 (57841130104)

    NDC Package Code 57841-1301-4
    Billing NDC 57841130104
    Package 1 BLISTER PACK in 1 CARTON (57841-1301-4) / 3 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2020-10-01
    NDC Exclude Flag N
    Pricing Information N/A