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    NDC 71335-0909-04 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 Bryant Ranch Prepack. The primary component is METHOCARBAMOL.

    Product Information

    NDC 71335-0909
    Product ID 71335-0909_65c460f6-6470-41ff-abb4-d9d54ecc52f7
    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 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 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 71335-0909-04 (71335090904)

    NDC Package Code 71335-0909-4
    Billing NDC 71335090904
    Package 120 TABLET, COATED in 1 BOTTLE (71335-0909-4)
    Marketing Start Date 2018-08-08
    NDC Exclude Flag N
    Pricing Information N/A