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    NDC 00093-1921-06 Cyclobenzaprine Hydrochloride 30 mg/1 Details

    Cyclobenzaprine Hydrochloride 30 mg/1

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

    Product Information

    NDC 00093-1921
    Product ID 0093-1921_a7cfb9fd-4417-4319-85c6-92c6fcad4085
    Associated GPIs 75100050107030
    GCN Sequence Number 062178
    GCN Sequence Number Description cyclobenzaprine HCl CAP ER 24H 30 MG ORAL
    HIC3 H6H
    HIC3 Description SKELETAL MUSCLE RELAXANTS
    GCN 97960
    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 30
    Active Ingredient Units mg/1
    Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
    Labeler Name Teva Pharmaceuticals USA, Inc.
    Pharmaceutical Class Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA021777
    Listing Certified Through 2024-12-31

    Package

    NDC 00093-1921-06 (00093192106)

    NDC Package Code 0093-1921-06
    Billing NDC 00093192106
    Package 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0093-1921-06)
    Marketing Start Date 2019-03-04
    NDC Exclude Flag N
    Pricing Information N/A