Package 87063-034-10
Brand: oxycodone and acetaminophen
Generic: oxycodone and acetaminophenPackage Facts
Identity
Package NDC
87063-034-10
Digits Only
8706303410
Product NDC
87063-034
Description
10 TABLET in 1 BOTTLE (87063-034-10)
Marketing
Marketing Status
Brand
oxycodone and acetaminophen
Generic
oxycodone and acetaminophen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44677216-216d-f82c-e063-6294a90a3dca", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["e0d06ec7-9846-4e04-8660-5fd6b2b8e423"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (87063-034-01)", "package_ndc": "87063-034-01", "marketing_start_date": "20251125"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (87063-034-05)", "package_ndc": "87063-034-05", "marketing_start_date": "20251125"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (87063-034-10)", "package_ndc": "87063-034-10", "marketing_start_date": "20251125"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (87063-034-20)", "package_ndc": "87063-034-20", "marketing_start_date": "20251125"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (87063-034-30)", "package_ndc": "87063-034-30", "marketing_start_date": "20251125"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (87063-034-60)", "package_ndc": "87063-034-60", "marketing_start_date": "20251125"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (87063-034-90)", "package_ndc": "87063-034-90", "marketing_start_date": "20251125"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "87063-034_44677216-216d-f82c-e063-6294a90a3dca", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "87063-034", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA207510", "marketing_category": "ANDA", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}