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    NDC 10702-0184-50 Oxycodone and Acetaminophen 325; 2.5 mg/1; mg/1 Details

    Oxycodone and Acetaminophen 325; 2.5 mg/1; mg/1

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

    Product Information

    NDC 10702-0184
    Product ID 10702-184_0bf26a01-454e-9d8b-e063-6294a90a9602
    Associated GPIs 65990002200305
    GCN Sequence Number 013998
    GCN Sequence Number Description oxycodone HCl/acetaminophen TABLET 2.5-325 MG ORAL
    HIC3 H3U
    HIC3 Description OPIOID ANALGESIC AND NON-SALICYLATE ANALGESICS
    GCN 70492
    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; 2.5
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; OXYCODONE
    Labeler Name KVK-Tech, Inc.
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA210644
    Listing Certified Through 2024-12-31

    Package

    NDC 10702-0184-50 (10702018450)

    NDC Package Code 10702-184-50
    Billing NDC 10702018450
    Package 500 TABLET in 1 BOTTLE (10702-184-50)
    Marketing Start Date 2018-02-09
    NDC Exclude Flag N
    Pricing Information N/A