oxycodone hydrochloride and acetaminophen (60760-965)

Drug Facts

Product Profile

Brand Name oxycodone hydrochloride and acetaminophen

Generic Name oxycodone hydrochloride and acetaminophen

Labeler st. mary's medical park pharmacy

Dosage Form TABLET

Routes

ORAL

Active Ingredients

acetaminophen 325 mg/1, oxycodone hydrochloride 10 mg/1

Manufacturer

ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-965

Product ID 60760-965_40a8831f-60ae-fa65-e063-6394a90ade4b

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA209385

DEA Schedule cii

Listing Expiration 2026-12-31

Marketing Start 2017-12-04

Pharmacologic Class

Classes

full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60760965

Hyphenated Format 60760-965

Supplemental Identifiers

RxCUI

1049214

UNII

362O9ITL9D 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 and acetaminophen (source: ndc)

Generic Name oxycodone hydrochloride and acetaminophen (source: ndc)

Application Number ANDA209385 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

325 mg/1
10 mg/1

source: ndc

Packaging

60 TABLET in 1 BOTTLE, PLASTIC (60760-965-60)
90 TABLET in 1 BOTTLE, PLASTIC (60760-965-90)

source: ndc

Packages (2)

60760-965-60 60 TABLET in 1 BOTTLE, PLASTIC (60760-965-60) 60760-965-90 90 TABLET in 1 BOTTLE, PLASTIC (60760-965-90)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (10 mg/1)

Linked Drug Pages (1)

Oxycodone Hydrochloride and Acetaminophen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "40a8831f-60ae-fa65-e063-6394a90ade4b", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049214"], "spl_set_id": ["40a882d6-a4db-1ad9-e063-6394a90a7268"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-965-60)", "package_ndc": "60760-965-60", "marketing_start_date": "20251007"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-965-90)", "package_ndc": "60760-965-90", "marketing_start_date": "20251007"}], "brand_name": "Oxycodone Hydrochloride and Acetaminophen", "product_id": "60760-965_40a8831f-60ae-fa65-e063-6394a90ade4b", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-965", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride and Acetaminophen", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209385", "marketing_category": "ANDA", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}