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    NDC 70934-0429-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is METAXALONE.

    Product Information

    NDC 70934-0429
    Product ID 70934-429_cb8020b3-57a7-cd67-e053-2995a90accc1
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208774
    Listing Certified Through n/a

    Package

    NDC 70934-0429-30 (70934042930)

    NDC Package Code 70934-429-30
    Billing NDC 70934042930
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-429-30)
    Marketing Start Date 2020-02-26
    NDC Exclude Flag N
    Pricing Information N/A
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