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    NDC 68788-7685-09 Clonidine Hydrochloride 0.2 mg/1 Details

    Clonidine Hydrochloride 0.2 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 68788-7685
    Product ID 68788-7685_e706e15e-b0ae-4af3-962b-4d200cf6e1dc
    Associated GPIs 36201010100310
    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 0.2
    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 ANDA070975
    Listing Certified Through 2023-12-31

    Package

    NDC 68788-7685-09 (68788768509)

    NDC Package Code 68788-7685-9
    Billing NDC 68788768509
    Package 90 TABLET in 1 BOTTLE (68788-7685-9)
    Marketing Start Date 2020-04-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 34091a88-a288-4e97-893e-7730d89e7059 Details

    Revised: 4/2022