Package 42806-114-01

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 42806-114-01
Digits Only 4280611401
Product NDC 42806-114
Product ID 42806-114_5418fa2c-3b31-4aec-ad48-6ee7bff4dd27
Description

100 TABLET in 1 BOTTLE (42806-114-01)

Marketing

Marketing Status
Marketed Since 2018-07-02
Brand oxycodone and acetaminophen
Generic oxycodone and acetaminophen
Sample Package No

Linked Drug Pages (1)

Oxycodone and Acetaminophen ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5418fa2c-3b31-4aec-ad48-6ee7bff4dd27", "openfda": {"upc": ["0342806116012", "0342806115015"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["700a229f-dc2d-7086-e053-2991aa0aec91"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-114-01)", "package_ndc": "42806-114-01", "marketing_start_date": "20180702"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "42806-114_5418fa2c-3b31-4aec-ad48-6ee7bff4dd27", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42806-114", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203864", "marketing_category": "ANDA", "marketing_start_date": "20180702", "listing_expiration_date": "20261231"}