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    NDC 00406-0512-91 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 SpecGx LLC. The primary component is ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE.

    Product Information

    NDC 00406-0512
    Product ID 0406-0512_a2cb3498-ca57-429c-861a-bf77f8487297
    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 hydrochloride 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 SpecGx LLC
    Pharmaceutical Class Full Opioid Agonists [MoA], Opioid Agonist [EPC]
    DEA Schedule CII
    Marketing Category ANDA
    Application Number ANDA087463
    Listing Certified Through 2025-12-31

    Package

    NDC 00406-0512-91 (00406051291)

    NDC Package Code 0406-0512-91
    Billing NDC 00406051291
    Package 5000 TABLET in 1 PAIL (0406-0512-91)
    Marketing Start Date 1983-12-07
    NDC Exclude Flag N
    Pricing Information N/A