roxicodone

Generic: oxycodone hydrochloride

Labeler: specgx llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name roxicodone
Generic Name oxycodone hydrochloride
Labeler specgx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 30 mg/1

Manufacturer
SpecGx LLC

Identifiers & Regulatory

Product NDC 23635-582
Product ID 23635-582_c4519228-edfd-422f-876d-b5edd5ff7283
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA021011
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2000-08-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 23635582
Hyphenated Format 23635-582

Supplemental Identifiers

RxCUI
1049611 1049613 1049618 1049620
UPC
0323635582100 0323635581103
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 roxicodone (source: ndc)
Generic Name oxycodone hydrochloride (source: ndc)
Application Number NDA021011 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (23635-582-10)
source: ndc

Packages (1)

23635-582-10 100 TABLET in 1 BOTTLE, PLASTIC (23635-582-10)

Ingredients (1)

oxycodone hydrochloride (30 mg/1)

Linked Drug Pages (1)

Roxicodone ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "c4519228-edfd-422f-876d-b5edd5ff7283", "openfda": {"upc": ["0323635582100", "0323635581103"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049613", "1049618", "1049620"], "spl_set_id": ["5a8157d3-ba20-4abf-b0d4-6ad141b31d63"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (23635-582-10)", "package_ndc": "23635-582-10", "marketing_start_date": "20000831"}], "brand_name": "Roxicodone", "product_id": "23635-582_c4519228-edfd-422f-876d-b5edd5ff7283", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "23635-582", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Roxicodone", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "NDA021011", "marketing_category": "NDA", "marketing_start_date": "20000831", "listing_expiration_date": "20261231"}