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    NDC 72887-0682-03 oxycodone and acetaminophen 300; 7.5 mg/1; mg/1 Details

    oxycodone and acetaminophen 300; 7.5 mg/1; mg/1

    oxycodone and acetaminophen is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by FH2 Pharma LLC. The primary component is ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE.

    Product Information

    NDC 72887-0682
    Product ID 72887-682_fa570597-2943-f861-e053-6294a90ad9c1
    Associated GPIs 65990002200325
    GCN Sequence Number 060728
    GCN Sequence Number Description oxycodone HCl/acetaminophen TABLET 7.5-300 MG ORAL
    HIC3 H3U
    HIC3 Description OPIOID ANALGESIC AND NON-SALICYLATE ANALGESICS
    GCN 26955
    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 300; 7.5
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
    Labeler Name FH2 Pharma LLC
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA040608
    Listing Certified Through 2024-12-31

    Package

    NDC 72887-0682-03 (72887068203)

    NDC Package Code 72887-682-03
    Billing NDC 72887068203
    Package 30 TABLET in 1 BOTTLE (72887-682-03)
    Marketing Start Date 2021-03-02
    NDC Exclude Flag N
    Pricing Information N/A