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    NDC 43063-0905-60 Methocarbamol 750 mg/1 Details

    Methocarbamol 750 mg/1

    Methocarbamol is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is METHOCARBAMOL.

    Product Information

    NDC 43063-0905
    Product ID 43063-905_ffec48e6-a99b-6245-e053-6394a90ad47b
    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 Tablets
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 750
    Active Ingredient Units mg/1
    Substance Name METHOCARBAMOL
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209312
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0905-60 (43063090560)

    NDC Package Code 43063-905-60
    Billing NDC 43063090560
    Package 60 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-60)
    Marketing Start Date 2019-01-09
    NDC Exclude Flag N
    Pricing Information N/A