Package 63629-8890-1
Brand: oxycodone hydrochloride
Generic: oxycodone hydrochloridePackage Facts
Identity
Package NDC
63629-8890-1
Digits Only
6362988901
Product NDC
63629-8890
Description
30 TABLET in 1 BOTTLE (63629-8890-1)
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": "b3b46d94-05f5-4c5f-bd3c-ffb632e62e10", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049618"], "spl_set_id": ["ff7f1268-ddb7-4742-beee-8b12966fe8f9"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-8890-1)", "package_ndc": "63629-8890-1", "marketing_start_date": "20211011"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-8890-2)", "package_ndc": "63629-8890-2", "marketing_start_date": "20211011"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-8890-3)", "package_ndc": "63629-8890-3", "marketing_start_date": "20211011"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (63629-8890-4)", "package_ndc": "63629-8890-4", "marketing_start_date": "20211011"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "63629-8890_b3b46d94-05f5-4c5f-bd3c-ffb632e62e10", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-8890", "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"}