Package 72887-193-03

Brand: oxycodone and acetaminophen

Generic: oxycodone and acetaminophen
NDC Package

Package Facts

Identity

Package NDC 72887-193-03
Digits Only 7288719303
Product NDC 72887-193
Description

30 TABLET in 1 BOTTLE, PLASTIC (72887-193-03)

Marketing

Marketing Status
Marketed Since 2019-06-03
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": "29293789-d966-1f97-e063-6394a90abe03", "openfda": {"upc": ["0372887193039", "0372887682038", "0372887683035", "0372887681031"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1014599", "1014615", "1014632", "1037259"], "spl_set_id": ["88d97caf-bcf5-3cde-e053-2995a90acf4a"], "manufacturer_name": ["FH2 Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72887-193-03)", "package_ndc": "72887-193-03", "marketing_start_date": "20190603"}], "brand_name": "oxycodone and acetaminophen", "product_id": "72887-193_29293789-d966-1f97-e063-6394a90abe03", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72887-193", "dea_schedule": "CII", "generic_name": "oxycodone and acetaminophen", "labeler_name": "FH2 Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "oxycodone and acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA040608", "marketing_category": "ANDA", "marketing_start_date": "20190603", "listing_expiration_date": "20261231"}