Package 71335-0677-5
Brand: oxycodone hydrochloride
Generic: oxycodonePackage Facts
Identity
Package NDC
71335-0677-5
Digits Only
7133506775
Product NDC
71335-0677
Description
100 TABLET in 1 BOTTLE (71335-0677-5)
Marketing
Marketing Status
Brand
oxycodone hydrochloride
Generic
oxycodone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5594265a-34ae-4fc4-b57d-f27189660711", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["9da42120-0214-45cb-bb98-9a7739e72d43"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0677-1)", "package_ndc": "71335-0677-1", "marketing_start_date": "20180309"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0677-2)", "package_ndc": "71335-0677-2", "marketing_start_date": "20180227"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0677-3)", "package_ndc": "71335-0677-3", "marketing_start_date": "20180524"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0677-4)", "package_ndc": "71335-0677-4", "marketing_start_date": "20180430"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0677-5)", "package_ndc": "71335-0677-5", "marketing_start_date": "20240529"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-0677-6)", "package_ndc": "71335-0677-6", "marketing_start_date": "20240529"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-0677-7)", "package_ndc": "71335-0677-7", "marketing_start_date": "20240529"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-0677-8)", "package_ndc": "71335-0677-8", "marketing_start_date": "20240529"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71335-0677_5594265a-34ae-4fc4-b57d-f27189660711", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-0677", "dea_schedule": "CII", "generic_name": "Oxycodone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}