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    NDC 70934-0442-30 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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 70934-0442
    Product ID 70934-442_f1851d69-4b48-13f7-e053-2995a90af2c0
    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 Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208170
    Listing Certified Through n/a

    Package

    NDC 70934-0442-30 (70934044230)

    NDC Package Code 70934-442-30
    Billing NDC 70934044230
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-442-30)
    Marketing Start Date 2019-11-01
    NDC Exclude Flag N
    Pricing Information N/A