Package 60760-964-60
Brand: oxycodone hydrochloride and acetaminophen
Generic: oxycodone hydrochloride and acetaminophenPackage Facts
Identity
Package NDC
60760-964-60
Digits Only
6076096460
Product NDC
60760-964
Description
60 TABLET in 1 BOTTLE, PLASTIC (60760-964-60)
Marketing
Marketing Status
Brand
oxycodone hydrochloride and acetaminophen
Generic
oxycodone hydrochloride and acetaminophen
Sample Package
No
Linked Drug Pages (1)
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"}