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    NDC 29300-0413-10 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 Unichem Pharmaceuticals (USA), Inc.. The primary component is CYCLOBENZAPRINE HYDROCHLORIDE.

    Product Information

    NDC 29300-0413
    Product ID 29300-413_cc113cd6-8904-4485-b1b2-15dd5ff7468b
    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 Unichem Pharmaceuticals (USA), Inc.
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213324
    Listing Certified Through 2024-12-31

    Package

    NDC 29300-0413-10 (29300041310)

    NDC Package Code 29300-413-10
    Billing NDC 29300041310
    Package 1000 TABLET, FILM COATED in 1 BOTTLE (29300-413-10)
    Marketing Start Date 2020-09-30
    NDC Exclude Flag N
    Pricing Information N/A