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    NDC 71335-0910-08 Methocarbamol 500 mg/1 Details

    Methocarbamol 500 mg/1

    Methocarbamol is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is METHOCARBAMOL.

    Product Information

    NDC 71335-0910
    Product ID 71335-0910_5a9ba45f-d88f-49e9-b4f4-021d948214ec
    Associated GPIs 75100070000305
    GCN Sequence Number 004654
    GCN Sequence Number Description methocarbamol TABLET 500 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 17892
    HICL Sequence Number 001938
    HICL Sequence Number Description METHOCARBAMOL
    Brand/Generic Generic
    Proprietary Name Methocarbamol
    Proprietary Name Suffix n/a
    Non-Proprietary Name Methocarbamol Tablets
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 500
    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 ANDA209312
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0910-08 (71335091008)

    NDC Package Code 71335-0910-8
    Billing NDC 71335091008
    Package 120 TABLET, COATED in 1 BOTTLE (71335-0910-8)
    Marketing Start Date 2022-02-23
    NDC Exclude Flag N
    Pricing Information N/A