Package 71335-2126-8
Brand: oxycodone hydrochloride
Generic: oxycodone hydrochloridePackage Facts
Identity
Package NDC
71335-2126-8
Digits Only
7133521268
Product NDC
71335-2126
Description
28 TABLET in 1 BOTTLE (71335-2126-8)
Marketing
Marketing Status
Brand
oxycodone hydrochloride
Generic
oxycodone hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1aa823c3-7615-481c-ae22-3432032ed3ee", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["27124cdf-a3e8-474c-9c1e-6fa48f6ddc05"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2126-1)", "package_ndc": "71335-2126-1", "marketing_start_date": "20220718"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2126-2)", "package_ndc": "71335-2126-2", "marketing_start_date": "20220718"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2126-3)", "package_ndc": "71335-2126-3", "marketing_start_date": "20220718"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2126-4)", "package_ndc": "71335-2126-4", "marketing_start_date": "20220718"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2126-5)", "package_ndc": "71335-2126-5", "marketing_start_date": "20220718"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-2126-6)", "package_ndc": "71335-2126-6", "marketing_start_date": "20220718"}, {"sample": false, "description": "18 TABLET in 1 BOTTLE (71335-2126-7)", "package_ndc": "71335-2126-7", "marketing_start_date": "20220718"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (71335-2126-8)", "package_ndc": "71335-2126-8", "marketing_start_date": "20220718"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71335-2126_1aa823c3-7615-481c-ae22-3432032ed3ee", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-2126", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20170808", "listing_expiration_date": "20261231"}