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    NDC 71335-0771-01 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 Bryant Ranch Prepack. The primary component is METHOCARBAMOL.

    Product Information

    NDC 71335-0771
    Product ID 71335-0771_37fa8916-531b-43e9-ac97-113c6c570ab6
    Associated GPIs 75100070000310
    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 Bryant Ranch Prepack
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA085123
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-0771-01 (71335077101)

    NDC Package Code 71335-0771-1
    Billing NDC 71335077101
    Package 20 TABLET in 1 BOTTLE (71335-0771-1)
    Marketing Start Date 2005-09-07
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6a237e91-b344-41cb-84b7-9a205e1f1a7d Details

    Revised: 1/2020