oxycodone hydrochloride and acetaminophen

Generic: oxycodone hydrochloride and acetaminophen

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

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 7.5 mg/1

Manufacturer
ST. MARY'S MEDICAL PARK PHARMACY

Identifiers & Regulatory

Product NDC 60760-964
Product ID 60760-964_423ef275-aad7-d3c8-e063-6294a90af842
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 60760964
Hyphenated Format 60760-964

Supplemental Identifiers

RxCUI
1049225
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
  • 7.5 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (60760-964-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (60760-964-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (60760-964-90)
source: ndc

Packages (3)

60760-964-30 30 TABLET in 1 BOTTLE, PLASTIC (60760-964-30) 60760-964-60 60 TABLET in 1 BOTTLE, PLASTIC (60760-964-60) 60760-964-90 90 TABLET in 1 BOTTLE, PLASTIC (60760-964-90)

Ingredients (2)

acetaminophen (325 mg/1) oxycodone hydrochloride (7.5 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": "423ef275-aad7-d3c8-e063-6294a90af842", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["40a68a27-4422-5ba0-e063-6294a90ac550"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (60760-964-30)", "package_ndc": "60760-964-30", "marketing_start_date": "20251007"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (60760-964-60)", "package_ndc": "60760-964-60", "marketing_start_date": "20251007"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-964-90)", "package_ndc": "60760-964-90", "marketing_start_date": "20251028"}], "brand_name": "Oxycodone Hydrochloride and Acetaminophen", "product_id": "60760-964_423ef275-aad7-d3c8-e063-6294a90af842", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60760-964", "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": "7.5 mg/1"}], "application_number": "ANDA209385", "marketing_category": "ANDA", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}