Package 47781-265-05

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 47781-265-05
Digits Only 4778126505
Product NDC 47781-265
Product ID 47781-265_aa023689-6275-e0a0-ab08-d45edc45ec40
Description

500 TABLET in 1 BOTTLE (47781-265-05)

Marketing

Marketing Status
Marketed Since 2011-12-30
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Oxycodone hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "aa023689-6275-e0a0-ab08-d45edc45ec40", "openfda": {"upc": ["0347781264017", "0347781263010", "0347781265014"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621"], "spl_set_id": ["20bb6bb4-230a-c9c2-01d8-a6e9341e96ba"], "manufacturer_name": ["Alvogen, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (47781-265-01)", "package_ndc": "47781-265-01", "marketing_start_date": "20111230"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (47781-265-05)", "package_ndc": "47781-265-05", "marketing_start_date": "20111230"}], "brand_name": "Oxycodone hydrochloride", "product_id": "47781-265_aa023689-6275-e0a0-ab08-d45edc45ec40", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "47781-265", "dea_schedule": "CII", "generic_name": "Oxycodone hydrochloride", "labeler_name": "Alvogen, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA202116", "marketing_category": "ANDA", "marketing_start_date": "20111230", "listing_expiration_date": "20271231"}