oxycodone hcl

Generic: oxycodone hcl

Labeler: amneal pharmaceuticals ny llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hcl
Generic Name oxycodone hcl
Labeler amneal pharmaceuticals ny llc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 20 mg/1

Manufacturer
Amneal Pharmaceuticals NY LLC

Identifiers & Regulatory

Product NDC 69238-2296
Product ID 69238-2296_32e0a011-6ef8-4c45-b080-33acd76a1bea
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA022272
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2022-04-01

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 692382296
Hyphenated Format 69238-2296

Supplemental Identifiers

RxCUI
1860129 1860137 1860148 1860157
UPC
0369238229813 0369238230017 0369238229615 0369238229417
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 oxycodone hcl (source: ndc)
Generic Name oxycodone hcl (source: ndc)
Application Number NDA022272 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2296-1)
source: ndc

Packages (1)

69238-2296-1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2296-1)

Ingredients (1)

oxycodone hydrochloride (20 mg/1)

Linked Drug Pages (1)

Oxycodone HCl ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "32e0a011-6ef8-4c45-b080-33acd76a1bea", "openfda": {"upc": ["0369238229813", "0369238230017", "0369238229615", "0369238229417"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1860129", "1860137", "1860148", "1860157"], "spl_set_id": ["8220e596-f32e-49cf-a11c-0c79209c3633"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2296-1)", "package_ndc": "69238-2296-1", "marketing_start_date": "20220401"}], "brand_name": "Oxycodone HCl", "product_id": "69238-2296_32e0a011-6ef8-4c45-b080-33acd76a1bea", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "69238-2296", "dea_schedule": "CII", "generic_name": "Oxycodone HCl", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone HCl", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "NDA022272", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20220401", "listing_expiration_date": "20261231"}