oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1422
Product ID 71335-1422_09f97067-e0dd-4966-8b1f-77855c9e08dc
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091490
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2014-09-08

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351422
Hyphenated Format 71335-1422

Supplemental Identifiers

RxCUI
1049683
UNII
C1ENJ2TE6C

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name oxycodone hydrochloride (source: ndc)
Generic Name oxycodone hydrochloride (source: ndc)
Application Number ANDA091490 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (71335-1422-1)
  • 30 TABLET in 1 BOTTLE (71335-1422-2)
  • 60 TABLET in 1 BOTTLE (71335-1422-3)
  • 90 TABLET in 1 BOTTLE (71335-1422-4)
  • 40 TABLET in 1 BOTTLE (71335-1422-5)
  • 28 TABLET in 1 BOTTLE (71335-1422-6)
source: ndc

Packages (6)

71335-1422-1 120 TABLET in 1 BOTTLE (71335-1422-1) 71335-1422-2 30 TABLET in 1 BOTTLE (71335-1422-2) 71335-1422-3 60 TABLET in 1 BOTTLE (71335-1422-3) 71335-1422-4 90 TABLET in 1 BOTTLE (71335-1422-4) 71335-1422-5 40 TABLET in 1 BOTTLE (71335-1422-5) 71335-1422-6 28 TABLET in 1 BOTTLE (71335-1422-6)

Ingredients (1)

oxycodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "09f97067-e0dd-4966-8b1f-77855c9e08dc", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049683"], "spl_set_id": ["bb33bf7f-aa70-4e8a-91b2-4e0400dc328e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1422-1)", "package_ndc": "71335-1422-1", "marketing_start_date": "20200306"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1422-2)", "package_ndc": "71335-1422-2", "marketing_start_date": "20191122"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1422-3)", "package_ndc": "71335-1422-3", "marketing_start_date": "20200306"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1422-4)", "package_ndc": "71335-1422-4", "marketing_start_date": "20191021"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1422-5)", "package_ndc": "71335-1422-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-1422-6)", "package_ndc": "71335-1422-6", "marketing_start_date": "20240709"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71335-1422_09f97067-e0dd-4966-8b1f-77855c9e08dc", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1422", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}