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    NDC 43386-0432-03 Oxycodone Hydrochloride 5 mg/1 Details

    Oxycodone Hydrochloride 5 mg/1

    Oxycodone Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lupin Pharmaceuticals,Inc.. The primary component is OXYCODONE HYDROCHLORIDE.

    Product Information

    NDC 43386-0432
    Product ID 43386-432_5fe9f019-fa7e-4ca8-ae55-a5ac54f1c7c4
    Associated GPIs 65100075100310
    GCN Sequence Number 004225
    GCN Sequence Number Description oxycodone HCl TABLET 5 MG ORAL
    HIC3 H3A
    HIC3 Description OPIOID ANALGESICS
    GCN 16290
    HICL Sequence Number 001742
    HICL Sequence Number Description OXYCODONE HCL
    Brand/Generic Generic
    Proprietary Name Oxycodone Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Oxycodone Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name OXYCODONE HYDROCHLORIDE
    Labeler Name Lupin Pharmaceuticals,Inc.
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA204021
    Listing Certified Through 2024-12-31

    Package

    NDC 43386-0432-03 (43386043203)

    NDC Package Code 43386-432-03
    Billing NDC 43386043203
    Package 30 TABLET in 1 BOTTLE (43386-432-03)
    Marketing Start Date 2017-06-12
    NDC Exclude Flag N
    Pricing Information N/A