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    NDC 51655-0575-20 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 Northwind Pharmaceuticals. The primary component is METHOCARBAMOL.

    Product Information

    NDC 51655-0575
    Product ID 51655-575_df63611f-90e5-6bbe-e053-2a95a90a2aad
    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 Northwind Pharmaceuticals
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090200
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0575-20 (51655057520)

    NDC Package Code 51655-575-20
    Billing NDC 51655057520
    Package 20 TABLET in 1 BOTTLE, PLASTIC (51655-575-20)
    Marketing Start Date 2020-08-24
    NDC Exclude Flag N
    Pricing Information N/A