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    NDC 68788-8172-03 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 Preferred Pharmaceuticals Inc.. The primary component is METHOCARBAMOL.

    Product Information

    NDC 68788-8172
    Product ID 68788-8172_8a381378-265e-40b4-9059-bca4b582b46b
    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 Preferred 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 68788-8172-03 (68788817203)

    NDC Package Code 68788-8172-3
    Billing NDC 68788817203
    Package 30 TABLET, COATED in 1 BOTTLE (68788-8172-3)
    Marketing Start Date 2022-04-25
    NDC Exclude Flag N
    Pricing Information N/A