Package 67296-2188-1

Brand: oxycodone hydrochloride

Generic: oxycodone hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67296-2188-1
Digits Only 6729621881
Product NDC 67296-2188
Product ID 67296-2188_44f3146e-88e3-80e1-e063-6394a90a3a28
Description

12 TABLET in 1 BOTTLE, PLASTIC (67296-2188-1)

Marketing

Marketing Status
Marketed Since 2024-09-10
Brand oxycodone hydrochloride
Generic oxycodone hydrochloride
Sample Package No

Linked Drug Pages (1)

Oxycodone Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44f3146e-88e3-80e1-e063-6394a90a3a28", "openfda": {"upc": ["0364380262015", "0364380260011", "0364380259015", "0364380261018", "0364380263012"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049621"], "spl_set_id": ["439c2de6-3ea5-e829-e063-6294a90aa77d"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE, PLASTIC (67296-2188-1)", "package_ndc": "67296-2188-1", "marketing_start_date": "20240910"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "67296-2188_44f3146e-88e3-80e1-e063-6394a90a3a28", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67296-2188", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA077712", "marketing_category": "ANDA", "marketing_start_date": "20240910", "listing_expiration_date": "20261231"}