Package 42806-007-01

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-007-01
Digits Only 4280600701
Product NDC 42806-007
Product ID 42806-007_5759388a-06ad-4a70-bd43-9c4abf69bc88
Description

100 TABLET in 1 BOTTLE (42806-007-01)

Marketing

Marketing Status
Marketed Since 2015-09-22
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": "5759388a-06ad-4a70-bd43-9c4abf69bc88", "openfda": {"upc": ["0342806007013", "0342806008010", "0342806009017", "0342806006016"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["cff1eee3-7c02-4f6c-acc5-1f6dcbab92c0"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-007-01)", "package_ndc": "42806-007-01", "marketing_start_date": "20150922"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "42806-007_5759388a-06ad-4a70-bd43-9c4abf69bc88", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42806-007", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "15 mg/1"}], "application_number": "ANDA202662", "marketing_category": "ANDA", "marketing_start_date": "20150922", "listing_expiration_date": "20261231"}