oxycodone hydrochloride

Generic: oxycodone hydrochloride

Labeler: st. mary's medical park pharmacy
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride
Generic Name oxycodone hydrochloride
Labeler st. mary's medical park pharmacy
Dosage Form TABLET
Routes
ORAL
Active Ingredients

oxycodone hydrochloride 5 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-954
Product ID 60760-954_3ccf459a-fb12-e137-e063-6394a90a5a80
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091393
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2013-10-18

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760954
Hyphenated Format 60760-954

Supplemental Identifiers

RxCUI
1049621
UNII
C1ENJ2TE6C

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 ANDA091393 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (60760-954-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (60760-954-60)
source: ndc

Packages (2)

60760-954-30 30 TABLET in 1 BOTTLE, PLASTIC (60760-954-30) 60760-954-60 60 TABLET in 1 BOTTLE, PLASTIC (60760-954-60)

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": "3ccf459a-fb12-e137-e063-6394a90a5a80", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["3ccf459a-fb11-e137-e063-6394a90a5a80"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-954-30)", "package_ndc": "60760-954-30", "marketing_start_date": "20250820"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-954-60)", "package_ndc": "60760-954-60", "marketing_start_date": "20250820"}], "brand_name": "OXYCODONE HYDROCHLORIDE", "product_id": "60760-954_3ccf459a-fb12-e137-e063-6394a90a5a80", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-954", "dea_schedule": "CII", "generic_name": "OXYCODONE HYDROCHLORIDE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA091393", "marketing_category": "ANDA", "marketing_start_date": "20131018", "listing_expiration_date": "20261231"}