oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: xlcare pharmaceuticals, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler xlcare pharmaceuticals, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 30 mg/1

Manufacturer
XLCare Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 72865-129
Product ID 72865-129_6261bbcf-f814-4219-9954-8f4662cfa9d9
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207418
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2020-02-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72865129
Hyphenated Format 72865-129

Supplemental Identifiers

RxCUI
1049611 1049618
UPC
0372865129012 0372865128015 0372865128053 0372865129050
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 ANDA207418 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72865-129-01)
  • 500 TABLET in 1 BOTTLE (72865-129-05)
source: ndc

Packages (2)

72865-129-01 100 TABLET in 1 BOTTLE (72865-129-01) 72865-129-05 500 TABLET in 1 BOTTLE (72865-129-05)

Ingredients (1)

oxycodone hydrochloride (30 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": "6261bbcf-f814-4219-9954-8f4662cfa9d9", "openfda": {"upc": ["0372865129012", "0372865128015", "0372865128053", "0372865129050"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618"], "spl_set_id": ["e5c8e72d-4ac5-4ca3-9557-6a659d4d8338"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-129-01)", "package_ndc": "72865-129-01", "marketing_start_date": "20200225"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-129-05)", "package_ndc": "72865-129-05", "marketing_start_date": "20200225"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "72865-129_6261bbcf-f814-4219-9954-8f4662cfa9d9", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72865-129", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "XLCare Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20200225", "listing_expiration_date": "20261231"}