Package 0054-0284-25

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0054-0284-25
Digits Only 0054028425
Product NDC 0054-0284
Product ID 0054-0284_74519e3e-078f-42ea-882e-1df0eb0eaaee
Description

100 TABLET in 1 BOTTLE (0054-0284-25)

Marketing

Marketing Status
Marketed Since 2010-09-27
Brand oxymorphone hydrochloride
Generic oxymorphone hydrochloride
Sample Package No

Linked Drug Pages (1)

Oxymorphone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "74519e3e-078f-42ea-882e-1df0eb0eaaee", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["3eb971cf-ab82-49f3-a46c-4d76a8ce599e"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0054-0284-25)", "package_ndc": "0054-0284-25", "marketing_start_date": "20100927"}], "brand_name": "Oxymorphone Hydrochloride", "product_id": "0054-0284_74519e3e-078f-42ea-882e-1df0eb0eaaee", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-0284", "dea_schedule": "CII", "generic_name": "oxymorphone hydrochloride", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxymorphone Hydrochloride", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090964", "marketing_category": "ANDA", "marketing_start_date": "20100927", "listing_expiration_date": "20261231"}