Package 71335-1959-4

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 71335-1959-4
Digits Only 7133519594
Product NDC 71335-1959
Description

30 TABLET in 1 BOTTLE (71335-1959-4)

Marketing

Marketing Status
Marketed Since 2021-10-26
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": "6eeeb7dc-4dfc-4cb4-99cf-ffcee9112f00", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["88d05136-7b04-4b25-af1c-6bc72fdbcbd7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-1959-1)", "package_ndc": "71335-1959-1", "marketing_start_date": "20240531"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (71335-1959-2)", "package_ndc": "71335-1959-2", "marketing_start_date": "20210930"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1959-3)", "package_ndc": "71335-1959-3", "marketing_start_date": "20240531"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1959-4)", "package_ndc": "71335-1959-4", "marketing_start_date": "20211026"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-1959-5)", "package_ndc": "71335-1959-5", "marketing_start_date": "20240531"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1959-6)", "package_ndc": "71335-1959-6", "marketing_start_date": "20211007"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1959-7)", "package_ndc": "71335-1959-7", "marketing_start_date": "20211026"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1959-8)", "package_ndc": "71335-1959-8", "marketing_start_date": "20211110"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "71335-1959_6eeeb7dc-4dfc-4cb4-99cf-ffcee9112f00", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1959", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYCODONE AND ACETAMINOPHEN", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "7.5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}