Package 31722-929-01

Brand: oxymorphone hydrochloride

Generic: oxymorphone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-929-01
Digits Only 3172292901
Product NDC 31722-929
Product ID 31722-929_53da63d9-6ef9-4feb-b704-5b7ef1785f6c
Description

100 TABLET in 1 BOTTLE (31722-929-01)

Marketing

Marketing Status
Marketed Since 2018-03-01
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": "53da63d9-6ef9-4feb-b704-5b7ef1785f6c", "openfda": {"upc": ["0331722930017", "0331722929011"], "unii": ["5Y2EI94NBC"], "rxcui": ["977939", "977942"], "spl_set_id": ["06af7dff-c261-4c03-9cd9-0605c42507fa"], "manufacturer_name": ["Camber Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-929-01)", "package_ndc": "31722-929-01", "marketing_start_date": "20180301"}], "brand_name": "OXYMORPHONE HYDROCHLORIDE", "product_id": "31722-929_53da63d9-6ef9-4feb-b704-5b7ef1785f6c", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-929", "dea_schedule": "CII", "generic_name": "OXYMORPHONE HYDROCHLORIDE", "labeler_name": "Camber 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": "20180301", "listing_expiration_date": "20261231"}