Package 65162-047-50

Brand: oxycodone hydrochloride

Generic: oxycodone
NDC Package

Package Facts

Identity

Package NDC 65162-047-50
Digits Only 6516204750
Product NDC 65162-047
Product ID 65162-047_8b9e3253-7735-44cc-a59b-3125ab573c84
Description

500 TABLET in 1 BOTTLE (65162-047-50)

Marketing

Marketing Status
Marketed Since 2012-10-30
Brand oxycodone hydrochloride
Generic oxycodone
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8b9e3253-7735-44cc-a59b-3125ab573c84", "openfda": {"upc": ["0365162049107", "0365162048100", "0365162047103", "0365162051032", "0365162050035", "0365162048032", "0365162049039", "0365162050103", "0365162051100", "0365162047035"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["094b64b3-cd32-4de5-afb6-ea00d9caad74"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-047-03)", "package_ndc": "65162-047-03", "marketing_start_date": "20121030"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-047-10)", "package_ndc": "65162-047-10", "marketing_start_date": "20121030"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (65162-047-25)", "package_ndc": "65162-047-25", "marketing_start_date": "20121030"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-047-50)", "package_ndc": "65162-047-50", "marketing_start_date": "20121030"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "65162-047_8b9e3253-7735-44cc-a59b-3125ab573c84", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "65162-047", "dea_schedule": "CII", "generic_name": "Oxycodone", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}