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    NDC 68788-7973-09 Methocarbamol 500 mg/1 Details

    Methocarbamol 500 mg/1

    Methocarbamol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc. The primary component is METHOCARBAMOL.

    Product Information

    NDC 68788-7973
    Product ID 68788-7973_3b72f17b-9c55-42ff-8c3b-df47535be470
    Associated GPIs 75100070000305
    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 Methocarbamol
    Proprietary Name Suffix n/a
    Non-Proprietary Name methocarbamol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METHOCARBAMOL
    Labeler Name Preferred Pharmaceuticals, Inc
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040489
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7973-09 (68788797309)

    NDC Package Code 68788-7973-9
    Billing NDC 68788797309
    Package 90 TABLET in 1 BOTTLE (68788-7973-9)
    Marketing Start Date 2021-07-28
    NDC Exclude Flag N
    Pricing Information N/A