Search by Drug Name or NDC

    NDC 50742-0247-05 Clonidine 0.1 mg/1 Details

    Clonidine 0.1 mg/1

    Clonidine is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ingenus Pharmaceuticals, LLC. The primary component is CLONIDINE HYDROCHLORIDE.

    Product Information

    NDC 50742-0247
    Product ID 50742-247_68a03cb8-23e0-4326-8a73-2838c11029a8
    Associated GPIs 61353020107420
    GCN Sequence Number 066895
    GCN Sequence Number Description clonidine HCl TAB ER 12H 0.1 MG ORAL
    HIC3 H8M
    HIC3 Description TX FOR ADHD - SELECTIVE ALPHA-2 RECEPTOR AGONIST
    GCN 29319
    HICL Sequence Number 000113
    HICL Sequence Number Description CLONIDINE HCL
    Brand/Generic Generic
    Proprietary Name Clonidine
    Proprietary Name Suffix n/a
    Non-Proprietary Name clonidine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 0.1
    Active Ingredient Units mg/1
    Substance Name CLONIDINE HYDROCHLORIDE
    Labeler Name Ingenus Pharmaceuticals, LLC
    Pharmaceutical Class Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209675
    Listing Certified Through 2024-12-31

    Package

    NDC 50742-0247-05 (50742024705)

    NDC Package Code 50742-247-05
    Billing NDC 50742024705
    Package 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50742-247-05)
    Marketing Start Date 2019-03-05
    NDC Exclude Flag N
    Pricing Information N/A