Package 63629-8889-4

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8889-4
Digits Only 6362988894
Product NDC 63629-8889
Description

120 TABLET in 1 BOTTLE (63629-8889-4)

Marketing

Marketing Status
Marketed Since 2021-10-21
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": "a1c4b9cd-2eb0-4e78-a5e1-e3e10f7a56bd", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049611"], "spl_set_id": ["7ec1ff9d-221f-463e-b2d4-5a0360b9c4d2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8889-1)", "package_ndc": "63629-8889-1", "marketing_start_date": "20211021"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-8889-2)", "package_ndc": "63629-8889-2", "marketing_start_date": "20211021"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-8889-3)", "package_ndc": "63629-8889-3", "marketing_start_date": "20211021"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63629-8889-4)", "package_ndc": "63629-8889-4", "marketing_start_date": "20211021"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "63629-8889_a1c4b9cd-2eb0-4e78-a5e1-e3e10f7a56bd", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8889", "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": "15 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20170808", "listing_expiration_date": "20261231"}