Package 72865-115-01

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72865-115-01
Digits Only 7286511501
Product NDC 72865-115
Description

100 TABLET in 1 BOTTLE (72865-115-01)

Marketing

Marketing Status
Marketed Since 2019-03-15
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": "9194f464-1cd1-44ac-8758-ae96b6643d5e", "openfda": {"upc": ["0372865113059", "0372865116050", "0372865113011", "0372865115053", "0372865115015", "0372865114056", "0372865116012", "0372865114018"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["7f3c6dd7-6bc8-450e-aded-997f9cf63a8f"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-115-01)", "package_ndc": "72865-115-01", "marketing_start_date": "20190315"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-115-05)", "package_ndc": "72865-115-05", "marketing_start_date": "20190315"}], "brand_name": "OXYCODONE AND ACETAMINOPHEN", "product_id": "72865-115_9194f464-1cd1-44ac-8758-ae96b6643d5e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72865-115", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "XLCare Pharmaceuticals, Inc.", "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"}