Package 63629-1926-1

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1926-1
Digits Only 6362919261
Product NDC 63629-1926
Product ID 63629-1926_c58a9e13-1792-4569-a677-28d9aaf0c9f0
Description

100 TABLET in 1 BOTTLE (63629-1926-1)

Marketing

Marketing Status
Marketed Since 2021-01-14
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": "c58a9e13-1792-4569-a677-28d9aaf0c9f0", "openfda": {"unii": ["5Y2EI94NBC"], "rxcui": ["977939"], "spl_set_id": ["560e9425-dfcb-4fb4-a759-b1e3f8f40fdb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1926-1)", "package_ndc": "63629-1926-1", "marketing_start_date": "20210114"}], "brand_name": "OXYMORPHONE HYDROCHLORIDE", "product_id": "63629-1926_c58a9e13-1792-4569-a677-28d9aaf0c9f0", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63629-1926", "dea_schedule": "CII", "generic_name": "OXYMORPHONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "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": "20180301", "listing_expiration_date": "20261231"}