oxycontin

Generic: oxycodone hydrochloride

Labeler: purdue pharma lp
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycontin
Generic Name oxycodone hydrochloride
Labeler purdue pharma lp
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 80 mg/1

Manufacturer
Purdue Pharma LP

Identifiers & Regulatory

Product NDC 59011-480
Product ID 59011-480_fee11108-8569-42d8-9e41-e49906b7a0be
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022272
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2010-08-08

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59011480
Hyphenated Format 59011-480

Supplemental Identifiers

RxCUI
1049504 1049545 1049565 1049576 1049586 1049595 1049601 1860127 1860129 1860137 1860148 1860151 1860154 1860157
UNII
C1ENJ2TE6C

Packaging Origin

Original Packager
true

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 oxycontin (source: ndc)
Generic Name oxycodone hydrochloride (source: ndc)
Application Number NDA022272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 80 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-480-10)
  • 2 BLISTER PACK in 1 CARTON (59011-480-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

59011-480-10 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-480-10) 59011-480-20 2 BLISTER PACK in 1 CARTON (59011-480-20) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (1)

oxycodone hydrochloride (80 mg/1)

Linked Drug Pages (1)

OxyContin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "fee11108-8569-42d8-9e41-e49906b7a0be", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049504", "1049545", "1049565", "1049576", "1049586", "1049595", "1049601", "1860127", "1860129", "1860137", "1860148", "1860151", "1860154", "1860157"], "spl_set_id": ["bfdfe235-d717-4855-a3c8-a13d26dadede"], "manufacturer_name": ["Purdue Pharma LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-480-10)", "package_ndc": "59011-480-10", "marketing_start_date": "20100808"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (59011-480-20)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59011-480-20", "marketing_start_date": "20100808"}], "brand_name": "OxyContin", "product_id": "59011-480_fee11108-8569-42d8-9e41-e49906b7a0be", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "59011-480", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "Purdue Pharma LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OxyContin", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "80 mg/1"}], "application_number": "NDA022272", "marketing_category": "NDA", "marketing_start_date": "20100808", "listing_expiration_date": "20271231"}