NDC 57664-224

oxycodone hydrochloride

Oxycodone Hydrochloride

oxycodone hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Oxycodone Hydrochloride.

Product ID57664-224_0aa4388a-fe20-4c91-a598-5e2698b75fc6
NDC57664-224
Product TypeHuman Prescription Drug
Proprietary Nameoxycodone hydrochloride
Generic NameOxycodone Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2009-05-12
Marketing CategoryANDA / ANDA
Application NumberANDA090659
Labeler NameSun Pharmaceutical Industries, Inc.
Substance NameOXYCODONE HYDROCHLORIDE
Active Ingredient Strength30 mg/1
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 57664-224-88

100 TABLET in 1 BOTTLE (57664-224-88)
Marketing Start Date2009-05-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57664-224-88 [57664022488]

oxycodone hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA090659
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2009-05-12

NDC 57664-224-08 [57664022408]

oxycodone hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA090659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-05-12
Marketing End Date2012-11-15

NDC 57664-224-13 [57664022413]

oxycodone hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA090659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-05-12
Marketing End Date2012-11-15

NDC 57664-224-83 [57664022483]

oxycodone hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA090659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-05-12
Marketing End Date2012-11-15

NDC 57664-224-18 [57664022418]

oxycodone hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA090659
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2009-05-12
Marketing End Date2012-11-15

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE30 mg/1

OpenFDA Data

SPL SET ID:11eddb9e-1cd6-4205-a3ce-c595c88e9d55
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049618
  • 1049611
  • 1049621
  • 1049683
  • 1049686
    • UPC Code
  • 0357664371886
  • 0357664370889

    • Pharmacological Class

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

    Medicade Reported Pricing

    57664022488 OXYCODONE HCL 30 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "oxycodone hydrochloride" or generic name "Oxycodone Hydrochloride"

    NDCBrand NameGeneric Name
    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
    68084-184Oxycodone HydrochlorideOxycodone Hydrochloride
    68084-354OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68084-185Oxycodone HydrochlorideOxycodone Hydrochloride
    68094-801Oxycodone HydrochlorideOxycodone Hydrochloride
    68084-975OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68084-828Oxycodone HydrochlorideOxycodone Hydrochloride
    68084-048Oxycodone HydrochlorideOxycodone Hydrochloride
    68084-983OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68084-968OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68094-005Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-108Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-020Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-505Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-120Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-111Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-145Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-110Oxycodone HydrochlorideOxycodone Hydrochloride
    68308-112Oxycodone HydrochlorideOxycodone Hydrochloride
    68382-793OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68382-795OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68382-794OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68382-797OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68382-796OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    68462-204Oxycodone HydrochlorideOxycodone Hydrochloride
    68462-347Oxycodone HydrochlorideOxycodone Hydrochloride
    0527-1774Oxycodone HydrochlorideOxycodone Hydrochloride
    0527-1426Oxycodone HydrochlorideOxycodone Hydrochloride
    70166-492Oxycodone HydrochlorideOxycodone Hydrochloride
    0591-2693Oxycodone HydrochlorideOxycodone Hydrochloride
    0591-2708Oxycodone HydrochlorideOxycodone Hydrochloride
    0603-4991Oxycodone HydrochlorideOxycodone Hydrochloride
    0603-4992Oxycodone HydrochlorideOxycodone Hydrochloride
    0603-4994Oxycodone HydrochlorideOxycodone Hydrochloride
    0603-4990Oxycodone HydrochlorideOxycodone Hydrochloride
    0603-4993Oxycodone HydrochlorideOxycodone Hydrochloride
    71335-0677Oxycodone HydrochlorideOxycodone Hydrochloride
    71335-0174OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
    71335-1023Oxycodone HydrochlorideOxycodone Hydrochloride
    71335-0209OXYCODONE HYDROCHLORIDEOXYCODONE HYDROCHLORIDE
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