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    NDC 71335-1099-09 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 Bryant Ranch Prepack. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 71335-1099
    Product ID 71335-1099_e1d36423-2d90-4161-933c-86e83e8c14a5
    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 Bryant Ranch Prepack
    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 71335-1099-09 (71335109909)

    NDC Package Code 71335-1099-9
    Billing NDC 71335109909
    Package 120 TABLET, FILM COATED in 1 BOTTLE (71335-1099-9)
    Marketing Start Date 2019-02-22
    NDC Exclude Flag N
    Pricing Information N/A