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    NDC 70518-3096-01 Methocarbamol 750 mg/1 Details

    Methocarbamol 750 mg/1

    Methocarbamol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is METHOCARBAMOL.

    Product Information

    NDC 70518-3096
    Product ID 70518-3096_07da099b-6b81-984d-e063-6294a90a12ac
    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 Methocarbamol
    Proprietary Name Suffix n/a
    Non-Proprietary Name methocarbamol
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name METHOCARBAMOL
    Labeler Name REMEDYREPACK 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 70518-3096-01 (70518309601)

    NDC Package Code 70518-3096-1
    Billing NDC 70518309601
    Package 90 TABLET in 1 BOTTLE, PLASTIC (70518-3096-1)
    Marketing Start Date 2021-05-26
    NDC Exclude Flag N
    Pricing Information N/A