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    NDC 72189-0283-20 CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 Details

    CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1

    CYCLOBENZAPRINE HYDROCHLORIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DirectRx. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 72189-0283
    Product ID 72189-283_ffc026bd-4962-46c6-e053-6394a90a6300
    Associated GPIs 75100050100303
    GCN Sequence Number 047478
    GCN Sequence Number Description cyclobenzaprine HCl TABLET 5 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 12805
    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 5
    Active Ingredient Units mg/1
    Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
    Labeler Name DirectRx
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208170
    Listing Certified Through 2024-12-31

    Package

    NDC 72189-0283-20 (72189028320)

    NDC Package Code 72189-283-20
    Billing NDC 72189028320
    Package 20 TABLET, FILM COATED in 1 BOTTLE (72189-283-20)
    Marketing Start Date 2021-10-19
    NDC Exclude Flag N
    Pricing Information N/A