Package 71335-1413-6

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1413-6
Digits Only 7133514136
Product NDC 71335-1413
Description

56 TABLET in 1 BOTTLE (71335-1413-6)

Marketing

Marketing Status
Marketed Since 2024-07-09
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46cc0480-4e5f-4cc6-ad38-0624d9456cdd", "openfda": {"unii": ["C1ENJ2TE6C"], "spl_set_id": ["1a190488-3444-43b0-b9c8-45c1eb371aad"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1413-1)", "package_ndc": "71335-1413-1", "marketing_start_date": "20200203"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1413-2)", "package_ndc": "71335-1413-2", "marketing_start_date": "20200706"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1413-3)", "package_ndc": "71335-1413-3", "marketing_start_date": "20200323"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1413-4)", "package_ndc": "71335-1413-4", "marketing_start_date": "20191231"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1413-5)", "package_ndc": "71335-1413-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-1413-6)", "package_ndc": "71335-1413-6", "marketing_start_date": "20240709"}, {"sample": false, "description": "84 TABLET in 1 BOTTLE (71335-1413-7)", "package_ndc": "71335-1413-7", "marketing_start_date": "20240709"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-1413-8)", "package_ndc": "71335-1413-8", "marketing_start_date": "20240709"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-1413-9)", "package_ndc": "71335-1413-9", "marketing_start_date": "20240709"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71335-1413_46cc0480-4e5f-4cc6-ad38-0624d9456cdd", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1413", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}