Package 31722-486-05

{"route": ["ORAL"], "spl_id": "a506a2bf-6041-4ed7-bf7c-ffe50b1b3c2e", "openfda": {"upc": ["0331722917018", "0331722485050", "0331722486019", "0331722918053", "0331722484053", "0331722486057", "0331722485012", "0331722917056", "0331722484015", "0331722918015"], "unii": ["C1ENJ2TE6C"], "rxcui": ["1049611", "1049618", "1049621", "1049683", "1049686"], "spl_set_id": ["01db4606-d49c-4b10-a78a-1cf41880a9fb"], "manufacturer_name": ["Camber Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-486-01)", "package_ndc": "31722-486-01", "marketing_start_date": "20251114"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-486-05)", "package_ndc": "31722-486-05", "marketing_start_date": "20251114"}], "brand_name": "Oxycodone Hydrochloride", "product_id": "31722-486_a506a2bf-6041-4ed7-bf7c-ffe50b1b3c2e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-486", "dea_schedule": "CII", "generic_name": "Oxycodone Hydrochloride", "labeler_name": "Camber Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone Hydrochloride", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA207418", "marketing_category": "ANDA", "marketing_start_date": "20251114", "listing_expiration_date": "20271231"}