Search by Drug Name or NDC

    NDC 63629-1926-01 OXYMORPHONE HYDROCHLORIDE 5 mg/1 Details

    OXYMORPHONE HYDROCHLORIDE 5 mg/1

    OXYMORPHONE HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is OXYMORPHONE HYDROCHLORIDE.

    Product Information

    NDC 63629-1926
    Product ID 63629-1926_c58a9e13-1792-4569-a677-28d9aaf0c9f0
    Associated GPIs 65100080100305
    GCN Sequence Number 061086
    GCN Sequence Number Description oxymorphone HCl TABLET 5 MG ORAL
    HIC3 H3A
    HIC3 Description OPIOID ANALGESICS
    GCN 27243
    HICL Sequence Number 001696
    HICL Sequence Number Description OXYMORPHONE HCL
    Brand/Generic Generic
    Proprietary Name OXYMORPHONE HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name OXYMORPHONE HYDROCHLORIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name OXYMORPHONE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA210175
    Listing Certified Through 2025-12-31

    Package

    NDC 63629-1926-01 (63629192601)

    NDC Package Code 63629-1926-1
    Billing NDC 63629192601
    Package 100 TABLET in 1 BOTTLE (63629-1926-1)
    Marketing Start Date 2021-01-14
    NDC Exclude Flag N
    Pricing Information N/A