Package 71335-9675-8
Brand: oxycodone and acetaminophen
Generic: oxycodone and acetaminophenPackage Facts
Identity
Package NDC
71335-9675-8
Digits Only
7133596758
Product NDC
71335-9675
Description
120 TABLET in 1 BOTTLE (71335-9675-8)
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": "3765101e-9311-474e-89eb-9e208c671c5a", "openfda": {"unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049225"], "spl_set_id": ["3339d3bd-b416-4c5b-8984-0c376544d8a9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (71335-9675-1)", "package_ndc": "71335-9675-1", "marketing_start_date": "20230327"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (71335-9675-2)", "package_ndc": "71335-9675-2", "marketing_start_date": "20230327"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-9675-3)", "package_ndc": "71335-9675-3", "marketing_start_date": "20230327"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9675-4)", "package_ndc": "71335-9675-4", "marketing_start_date": "20230327"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (71335-9675-5)", "package_ndc": "71335-9675-5", "marketing_start_date": "20230327"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-9675-6)", "package_ndc": "71335-9675-6", "marketing_start_date": "20230327"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-9675-7)", "package_ndc": "71335-9675-7", "marketing_start_date": "20230327"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-9675-8)", "package_ndc": "71335-9675-8", "marketing_start_date": "20230327"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "71335-9675_3765101e-9311-474e-89eb-9e208c671c5a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-9675", "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": "ANDA207510", "marketing_category": "ANDA", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}