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    NDC 45865-0987-60 Methocarbamol 500 mg/1 Details

    Methocarbamol 500 mg/1

    Methocarbamol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by medsource pharmaceuticals. The primary component is METHOCARBAMOL.

    Product Information

    NDC 45865-0987
    Product ID 45865-987_9af24216-c452-376c-e053-2a95a90aa613
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name METHOCARBAMOL
    Labeler Name medsource pharmaceuticals
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208507
    Listing Certified Through 2024-12-31

    Package

    NDC 45865-0987-60 (45865098760)

    NDC Package Code 45865-987-60
    Billing NDC 45865098760
    Package 60 TABLET, FILM COATED in 1 BOTTLE (45865-987-60)
    Marketing Start Date 2019-12-11
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9af244ce-8829-4443-e053-2995a90af4e3 Details

    Revised: 12/2019