Package 71335-1421-0

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-1421-0
Digits Only 7133514210
Product NDC 71335-1421
Description

15 TABLET in 1 BOTTLE (71335-1421-0)

Marketing

Marketing Status
Marketed Since 2024-07-02
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "86ab7d29-049d-4d6a-aad4-9d1664442d82", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["1bcddbe1-c453-43ec-a822-9e993b885a5f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE (71335-1421-0)", "package_ndc": "71335-1421-0", "marketing_start_date": "20240702"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1421-1)", "package_ndc": "71335-1421-1", "marketing_start_date": "20191213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1421-2)", "package_ndc": "71335-1421-2", "marketing_start_date": "20191216"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1421-3)", "package_ndc": "71335-1421-3", "marketing_start_date": "20191216"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-1421-4)", "package_ndc": "71335-1421-4", "marketing_start_date": "20240709"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1421-5)", "package_ndc": "71335-1421-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-1421-6)", "package_ndc": "71335-1421-6", "marketing_start_date": "20200921"}, {"sample": false, "description": "50 TABLET in 1 BOTTLE (71335-1421-7)", "package_ndc": "71335-1421-7", "marketing_start_date": "20240709"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (71335-1421-8)", "package_ndc": "71335-1421-8", "marketing_start_date": "20240709"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-1421-9)", "package_ndc": "71335-1421-9", "marketing_start_date": "20191206"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "71335-1421_86ab7d29-049d-4d6a-aad4-9d1664442d82", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-1421", "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": "5 mg/1"}], "application_number": "ANDA091490", "marketing_category": "ANDA", "marketing_start_date": "20140908", "listing_expiration_date": "20261231"}