NDC 63629-7399

OXYCODONE HYDROCHLORIDE

Oxycodone Hydrochloride

OXYCODONE HYDROCHLORIDE is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Oxycodone Hydrochloride.

Product ID63629-7399_32cbf6a0-3df6-47b0-aa70-75207fcbcca1
NDC63629-7399
Product TypeHuman Prescription Drug
Proprietary NameOXYCODONE HYDROCHLORIDE
Generic NameOxycodone Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-12-26
Marketing CategoryANDA / ANDA
Application NumberANDA077290
Labeler NameBryant Ranch Prepack
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 63629-7399-1

60 TABLET in 1 BOTTLE (63629-7399-1)
Marketing Start Date2017-09-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-7399-6 [63629739906]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA077290
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-05-31
Inactivation Date2020-01-31

NDC 63629-7399-3 [63629739903]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA077290
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20
Inactivation Date2020-01-31

NDC 63629-7399-4 [63629739904]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA077290
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-05-31
Inactivation Date2020-01-31

NDC 63629-7399-1 [63629739901]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA077290
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20
Inactivation Date2020-01-31

NDC 63629-7399-2 [63629739902]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA077290
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-20
Inactivation Date2020-01-31

NDC 63629-7399-5 [63629739905]

OXYCODONE HYDROCHLORIDE TABLET
Marketing CategoryANDA
Application NumberANDA077290
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-05-31
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE20 mg/1

OpenFDA Data

SPL SET ID:8cd841f7-9420-417f-9814-04dcb9b48737
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049683
  • 1049686
  • Pharmacological Class

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

    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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