Package 72865-130-01

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72865-130-01
Digits Only 7286513001
Product NDC 72865-130
Product ID 72865-130_4fdf3b7e-f6ff-4d78-a928-c9d47c5bc9d9
Description

100 TABLET in 1 BOTTLE (72865-130-01)

Marketing

Marketing Status
Marketed Since 2020-05-06
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": "4fdf3b7e-f6ff-4d78-a928-c9d47c5bc9d9", "openfda": {"upc": ["0372865131015", "0372865130018"], "unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["1a1d5061-b62a-49fa-a5b2-4970f51416ae"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72865-130-01)", "package_ndc": "72865-130-01", "marketing_start_date": "20200506"}], "brand_name": "OXYMORPHONE HYDROCHLORIDE", "product_id": "72865-130_4fdf3b7e-f6ff-4d78-a928-c9d47c5bc9d9", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72865-130", "dea_schedule": "CII", "generic_name": "OXYMORPHONE HYDROCHLORIDE", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXYMORPHONE HYDROCHLORIDE", "active_ingredients": [{"name": "OXYMORPHONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210175", "marketing_category": "ANDA", "marketing_start_date": "20200506", "listing_expiration_date": "20261231"}