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    NDC 68788-7675-09 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 Preferred Pharmaceuticals, Inc.. The primary component is METAXALONE.

    Product Information

    NDC 68788-7675
    Product ID 68788-7675_2559cfc3-459b-42ef-94d2-90322ed5e96c
    Associated GPIs 75100060000320
    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 Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204770
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7675-09 (68788767509)

    NDC Package Code 68788-7675-9
    Billing NDC 68788767509
    Package 90 TABLET in 1 BOTTLE (68788-7675-9)
    Marketing Start Date 2020-03-02
    NDC Exclude Flag N
    Pricing Information N/A
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