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    NDC 72865-0114-01 Oxycodone and Acetaminophen 325; 5 mg/1; mg/1 Details

    Oxycodone and Acetaminophen 325; 5 mg/1; mg/1

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

    Product Information

    NDC 72865-0114
    Product ID 72865-114_e95ef7d6-3a21-4846-b1fd-f15a87675304
    Associated GPIs 65990002200310
    GCN Sequence Number 004222
    GCN Sequence Number Description oxycodone HCl/acetaminophen TABLET 5 MG-325MG ORAL
    HIC3 H3U
    HIC3 Description OPIOID ANALGESIC AND NON-SALICYLATE ANALGESICS
    GCN 70491
    HICL Sequence Number 001741
    HICL Sequence Number Description OXYCODONE HCL/ACETAMINOPHEN
    Brand/Generic Generic
    Proprietary Name Oxycodone and Acetaminophen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Oxycodone and Acetaminophen
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 325; 5
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
    Labeler Name XLCare Pharmaceuticals, Inc.
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA207419
    Listing Certified Through 2024-12-31

    Package

    NDC 72865-0114-01 (72865011401)

    NDC Package Code 72865-114-01
    Billing NDC 72865011401
    Package 100 TABLET in 1 BOTTLE (72865-114-01)
    Marketing Start Date 2019-03-15
    NDC Exclude Flag N
    Pricing Information N/A