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    NDC 60505-3972-06 Cyclobenzaprine Hydrochloride 15 mg/1 Details

    Cyclobenzaprine Hydrochloride 15 mg/1

    Cyclobenzaprine Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Apotex Corp.. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 60505-3972
    Product ID 60505-3972_d5ad254d-7c8e-f25b-85d3-07dcbf61fac7
    Associated GPIs 75100050107015
    GCN Sequence Number 062177
    GCN Sequence Number Description cyclobenzaprine HCl CAP ER 24H 15 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 97959
    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 CAPSULE, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 15
    Active Ingredient Units mg/1
    Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
    Labeler Name Apotex Corp.
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA206703
    Listing Certified Through 2023-12-31

    Package

    NDC 60505-3972-06 (60505397206)

    NDC Package Code 60505-3972-6
    Billing NDC 60505397206
    Package 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (60505-3972-6)
    Marketing Start Date 2019-03-01
    NDC Exclude Flag N
    Pricing Information N/A