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    NDC 55700-0239-01 Cyclobenzaprine Hydrochloride 7.5 mg/1 Details

    Cyclobenzaprine Hydrochloride 7.5 mg/1

    Cyclobenzaprine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Quality Care Products LLC. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 55700-0239
    Product ID 55700-239_7b064e6b-5783-43ae-b61c-9c1c36b35099
    Associated GPIs 75100050100304
    GCN Sequence Number 062524
    GCN Sequence Number Description cyclobenzaprine HCl TABLET 7.5 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 98299
    HICL Sequence Number 001950
    HICL Sequence Number Description CYCLOBENZAPRINE HCL
    Brand/Generic Generic
    Proprietary Name Cyclobenzaprine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Cyclobenzaprine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 7.5
    Active Ingredient Units mg/1
    Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
    Labeler Name Quality Care Products LLC
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078722
    Listing Certified Through 2025-12-31

    Package

    NDC 55700-0239-01 (55700023901)

    NDC Package Code 55700-239-01
    Billing NDC 55700023901
    Package 120 TABLET, FILM COATED in 1 BOTTLE (55700-239-01)
    Marketing Start Date 2015-04-24
    NDC Exclude Flag N
    Pricing Information N/A