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    NDC 72789-0046-60 Cyclobenzaprine Hydrochloride 10 mg/1 Details

    Cyclobenzaprine Hydrochloride 10 mg/1

    Cyclobenzaprine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 72789-0046
    Product ID 72789-046_f8877d27-32fc-ade7-e053-6394a90abe9e
    Associated GPIs 75100050100305
    GCN Sequence Number 004681
    GCN Sequence Number Description cyclobenzaprine HCl TABLET 10 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 18020
    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 10
    Active Ingredient Units mg/1
    Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077797
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0046-60 (72789004660)

    NDC Package Code 72789-046-60
    Billing NDC 72789004660
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-046-60)
    Marketing Start Date 2020-01-06
    NDC Exclude Flag N
    Pricing Information N/A