oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: epic pharma, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler epic pharma, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
Epic Pharma, LLC

Identifiers & Regulatory

Product NDC 42806-005
Product ID 42806-005_5759388a-06ad-4a70-bd43-9c4abf69bc88
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202662
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2015-09-22

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42806005
Hyphenated Format 42806-005

Supplemental Identifiers

RxCUI
1049611 1049618 1049621 1049683 1049686
UPC
0342806007013 0342806008010 0342806009017 0342806006016
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 hydrochloride (source: ndc)
Generic Name oxycodone hydrochloride (source: ndc)
Application Number ANDA202662 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42806-005-01)
source: ndc

Packages (1)

42806-005-01 100 TABLET in 1 BOTTLE (42806-005-01)

Ingredients (1)

oxycodone hydrochloride (5 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": "5759388a-06ad-4a70-bd43-9c4abf69bc88", "openfda": {"upc": ["0342806007013", "0342806008010", "0342806009017", "0342806006016"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["cff1eee3-7c02-4f6c-acc5-1f6dcbab92c0"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-005-01)", "package_ndc": "42806-005-01", "marketing_start_date": "20150922"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "42806-005_5759388a-06ad-4a70-bd43-9c4abf69bc88", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42806-005", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA202662", "marketing_category": "ANDA", "marketing_start_date": "20150922", "listing_expiration_date": "20261231"}