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    NDC 51655-0171-52 Metaxalone 800 mg/1 Details

    Metaxalone 800 mg/1

    Metaxalone is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is METAXALONE.

    Product Information

    NDC 51655-0171
    Product ID 51655-171_f2b46c1a-bf96-1622-e053-2a95a90a91f0
    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 Metaxalone
    Proprietary Name Suffix n/a
    Non-Proprietary Name Metaxalone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 800
    Active Ingredient Units mg/1
    Substance Name METAXALONE
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207466
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0171-52 (51655017152)

    NDC Package Code 51655-171-52
    Billing NDC 51655017152
    Package 30 TABLET in 1 BOTTLE, PLASTIC (51655-171-52)
    Marketing Start Date 2023-02-03
    NDC Exclude Flag N
    Pricing Information N/A
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