Search by Drug Name or NDC

    NDC 50090-4164-03 Methocarbamol 750 mg/1 Details

    Methocarbamol 750 mg/1

    Methocarbamol is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is METHOCARBAMOL.

    Product Information

    NDC 50090-4164
    Product ID 50090-4164_035a2f96-916b-460a-9e9a-3309ee342d92
    Associated GPIs 75100070000310
    GCN Sequence Number 004655
    GCN Sequence Number Description methocarbamol TABLET 750 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 17893
    HICL Sequence Number 001938
    HICL Sequence Number Description METHOCARBAMOL
    Brand/Generic Generic
    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 750
    Active Ingredient Units mg/1
    Substance Name METHOCARBAMOL
    Labeler Name A-S Medication Solutions
    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 50090-4164-03 (50090416403)

    NDC Package Code 50090-4164-3
    Billing NDC 50090416403
    Package 30 TABLET, FILM COATED in 1 BOTTLE (50090-4164-3)
    Marketing Start Date 2019-06-12
    NDC Exclude Flag N
    Pricing Information N/A