NDC 0603-4979

Oxycodone and Acetaminophen

Oxycodone Hydrochloride And Acetaminophen

Oxycodone and Acetaminophen is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Par Pharmaceutical, Inc.. The primary component is Oxycodone Hydrochloride; Acetaminophen.

Product ID0603-4979_18d75374-066d-4bc1-8ab6-be4312a65b2c
NDC0603-4979
Product TypeHuman Prescription Drug
Proprietary NameOxycodone and Acetaminophen
Generic NameOxycodone Hydrochloride And Acetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2013-07-11
Marketing End Date2021-10-31
Marketing CategoryANDA / ANDA
Application NumberANDA090734
Labeler NamePar Pharmaceutical, Inc.
Substance NameOXYCODONE HYDROCHLORIDE; ACETAMINOPHEN
Active Ingredient Strength8 mg/1; mg/1
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN

Packaging

NDC 0603-4979-21

100 TABLET in 1 BOTTLE, PLASTIC (0603-4979-21)
Marketing Start Date2013-07-11
Marketing End Date2021-10-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0603-4979-21 [00603497921]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA090734
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-07-11

NDC 0603-4979-28 [00603497928]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA090734
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-07-11

NDC 0603-4979-32 [00603497932]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA090734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-07-11
Marketing End Date2016-01-27

NDC 0603-4979-10 [00603497910]

Oxycodone and Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA090734
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-07-11
Marketing End Date2016-01-27

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE7.5 mg/1

OpenFDA Data

SPL SET ID:c2520a5a-ef9c-47d0-82e7-12f2b23e154b
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049214
  • 1049225
    • UPC Code
  • 0306034979214
  • 0306034982214

    • Pharmacological Class

    • Full Opioid Agonists [MoA]
    • Opioid Agonist [EPC]

    NDC Crossover Matching brand name "Oxycodone and Acetaminophen" or generic name "Oxycodone Hydrochloride And Acetaminophen"

    NDCBrand NameGeneric Name
    0054-0551Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0228-2981Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0228-2982Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0228-2983Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0406-0512OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0406-0522OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0406-0523OXYCODONE AND ACETAMINOPHENoxycodone hydrochloride and acetaminophen
    0527-1669Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0527-1671Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0603-4978Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0603-4979Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0603-4982Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    0603-4998Oxycodone and AcetaminophenOxycodone hydrochloride and Acetaminophen
    68084-355Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68084-710Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68094-013Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68084-699Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-480Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-840Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-842Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-843Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-405Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-475Oxycodone and AcetaminophenOxycodone and Acetaminophen
    68308-841Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70700-105Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1327Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1328Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1329Oxycodone and AcetaminophenOxycodone and Acetaminophen
    70710-1330Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0146Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0216Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0193Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0221oxycodone and acetaminophenoxycodone and acetaminophen
    71335-1036Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0316Oxycodone and AcetaminophenOxycodone and Acetaminophen
    71335-0722Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0904-6438Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0904-6439Oxycodone and AcetaminophenOxycodone and Acetaminophen
    0904-6437Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10544-287OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHEN
    10702-187Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10544-621Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10702-238OXYCODONE AND ACETAMINOPHENOXYCODONE AND ACETAMINOPHEN
    10702-185Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10702-186Oxycodone and AcetaminophenOxycodone and Acetaminophen
    10702-184Oxycodone and AcetaminophenOxycodone and Acetaminophen
    13107-044Oxycodone and AcetaminophenOxycodone and Acetaminophen
    13107-043Oxycodone and AcetaminophenOxycodone and Acetaminophen
    12634-942Oxycodone and AcetaminophenOxycodone and Acetaminophen
    13107-045Oxycodone and AcetaminophenOxycodone and Acetaminophen
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