NDC 71335-1080

Oxycodone Hydrochloride

Oxycodone

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 ID71335-1080_3ddf2537-9837-4432-a80e-33a751f11a6b
NDC71335-1080
Product TypeHuman Prescription Drug
Proprietary NameOxycodone Hydrochloride
Generic NameOxycodone
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2012-10-30
Marketing CategoryANDA / ANDA
Application NumberANDA203638
Labeler NameBryant Ranch Prepack
Substance NameOXYCODONE HYDROCHLORIDE
Active Ingredient Strength15 mg/1
Pharm ClassesFull Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA ScheduleCII
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71335-1080-1

60 TABLET in 1 BOTTLE (71335-1080-1)
Marketing Start Date2019-02-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1080-4 [71335108004]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-6 [71335108006]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-9 [71335108009]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-3 [71335108003]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-5 [71335108005]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-8 [71335108008]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-2 [71335108002]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-7 [71335108007]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

NDC 71335-1080-1 [71335108001]

Oxycodone Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA203638
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-02-04

Drug Details

Active Ingredients

IngredientStrength
OXYCODONE HYDROCHLORIDE15 mg/1

OpenFDA Data

SPL SET ID:9da42120-0214-45cb-bb98-9a7739e72d43
Manufacturer
UNII

Pharmacological Class

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

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

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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