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    NDC 68788-7145-03 clonidine hydrochloride 0.1 mg/1 Details

    clonidine hydrochloride 0.1 mg/1

    clonidine hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is CLONIDINE HYDROCHLORIDE.

    Product Information

    NDC 68788-7145
    Product ID 68788-7145_584a6016-7cb6-4433-8287-6f01320ec911
    Associated GPIs 36201010100305
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name clonidine hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Clonidine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 0.1
    Active Ingredient Units mg/1
    Substance Name CLONIDINE HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091368
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7145-03 (68788714503)

    NDC Package Code 68788-7145-3
    Billing NDC 68788714503
    Package 30 TABLET in 1 BOTTLE (68788-7145-3)
    Marketing Start Date 2018-04-23
    NDC Exclude Flag N
    Pricing Information N/A