NDC 59011-420

OxyContin

Oxycodone Hydrochloride

OxyContin is a Oral Tablet, Film Coated, Extended Release in the Human Prescription Drug category. It is labeled and distributed by Purdue Pharma Lp. The primary component is Oxycodone Hydrochloride.

Product ID59011-420_21ec1aed-af99-6d71-bc44-4755651ecd9e
NDC59011-420
Product TypeHuman Prescription Drug
Proprietary NameOxyContin
Generic NameOxycodone Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2010-08-08
Marketing CategoryNDA / NDA
Application NumberNDA022272
Labeler NamePurdue Pharma LP
Substance NameOXYCODONE HYDROCHLORIDE
Active Ingredient Strength20 mg/1
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 59011-420-10

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-420-10)
Marketing Start Date2010-08-08
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 59011-420-10 [59011042010]

OxyContin TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA022272
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-08

NDC 59011-420-20 [59011042020]

OxyContin TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryNDA
Application NumberNDA022272
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-08-08

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:bfdfe235-d717-4855-a3c8-a13d26dadede
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1860148
  • 1049545
  • 1860151
  • 1860157
  • 1860154
  • 1049576
  • 1049565
  • 1049504
  • 1049586
  • 1860129
  • 1860127
  • 1049601
  • 1860137
  • 1049595
    • UPC Code
  • 0359011415106
  • 0359011480104
  • 0359011460106
  • 0359011410101
  • 0359011420100

    • Pharmacological Class

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

    Medicade Reported Pricing

    59011042020 OXYCONTIN ER 20 MG TABLET

    Pricing Unit: EA | Drug Type:

    59011042010 OXYCONTIN ER 20 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "OxyContin" or generic name "Oxycodone Hydrochloride"

    NDCBrand NameGeneric Name
    21695-951OxyContinOxyContin
    21695-941OxyContinOxyContin
    42254-159OxyContinOxyContin
    59011-410OxyContinOxyContin
    59011-415OxyContinOxyContin
    59011-430OxyContinOxyContin
    59011-440OxyContinOxyContin
    59011-480OxyContinOxyContin
    59011-460OxyContinOxyContin
    59011-420OxyContinOxyContin
    63629-3774OxyContinOxyContin
    0054-0390oxycodone hydrochlorideoxycodone hydrochloride
    0054-0393Oxycodone HydrochlorideOxycodone Hydrochloride
    0054-0522Oxycodone HydrochlorideOxycodone Hydrochloride
    0093-5731Oxycodone HydrochlorideOxycodone Hydrochloride
    0093-5732Oxycodone HydrochlorideOxycodone Hydrochloride
    0093-5733Oxycodone HydrochlorideOxycodone Hydrochloride
    0093-5734Oxycodone HydrochlorideOxycodone Hydrochloride
    0115-1556OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    0115-1557OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    0115-1558OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    0115-1559OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE

    Trademark Results [OxyContin]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    OXYCONTIN
    OXYCONTIN
    90470025 not registered Live/Pending
    Yangzhou Zhixing Network Technology Co., Ltd.
    2021-01-15
    OXYCONTIN
    OXYCONTIN
    75069553 2033914 Live/Registered
    PURDUE PHARMA L.P.
    1996-03-08
    OXYCONTIN
    OXYCONTIN
    74339006 2004586 Live/Registered
    PURDUE PHARMA L.P.
    1992-12-10
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