Package 42806-331-01

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42806-331-01
Digits Only 4280633101
Product NDC 42806-331
Product ID 42806-331_8a01b8b5-5114-46e2-9949-1ab6beb78d81
Description

100 TABLET in 1 BOTTLE (42806-331-01)

Marketing

Marketing Status
Marketed Since 2019-05-15
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": "8a01b8b5-5114-46e2-9949-1ab6beb78d81", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["95804e72-232d-425d-b23d-a66f43bdf0c6"], "manufacturer_name": ["Epic Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42806-331-01)", "package_ndc": "42806-331-01", "marketing_start_date": "20190515"}], "brand_name": "Oxymorphone Hydrochloride", "product_id": "42806-331_8a01b8b5-5114-46e2-9949-1ab6beb78d81", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42806-331", "dea_schedule": "CII", "generic_name": "Oxymorphone Hydrochloride", "labeler_name": "Epic Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxymorphone Hydrochloride", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201187", "marketing_category": "ANDA", "marketing_start_date": "20190515", "listing_expiration_date": "20261231"}