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    NDC 43386-0434-05 Oxycodone Hydrochloride 20 mg/1 Details

    Oxycodone Hydrochloride 20 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 43386-0434
    Product ID 43386-434_5fe9f019-fa7e-4ca8-ae55-a5ac54f1c7c4
    Associated GPIs 65100075100330
    GCN Sequence Number 045298
    GCN Sequence Number Description oxycodone HCl TABLET 20 MG ORAL
    HIC3 H3A
    HIC3 Description OPIOID ANALGESICS
    GCN 21194
    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 20
    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 43386-0434-05 (43386043405)

    NDC Package Code 43386-434-05
    Billing NDC 43386043405
    Package 500 TABLET in 1 BOTTLE (43386-434-05)
    Marketing Start Date 2017-06-12
    NDC Exclude Flag N
    Pricing Information N/A