Package 65162-048-03
Brand: oxycodone hydrochloride
Generic: oxycodonePackage Facts
Identity
Package NDC
65162-048-03
Digits Only
6516204803
Product NDC
65162-048
Description
30 TABLET in 1 BOTTLE (65162-048-03)
Marketing
Marketing Status
Brand
oxycodone hydrochloride
Generic
oxycodone
Sample Package
No
Linked Drug Pages (1)
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 (65162-048-03)", "package_ndc": "65162-048-03", "marketing_start_date": "20121030"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-048-10)", "package_ndc": "65162-048-10", "marketing_start_date": "20121030"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (65162-048-25)", "package_ndc": "65162-048-25", "marketing_start_date": "20121030"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "65162-048_8b9e3253-7735-44cc-a59b-3125ab573c84", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "65162-048", "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": "10 mg/1"}], "application_number": "ANDA203638", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}