Package 68071-5054-4

{"route": ["ORAL"], "spl_id": "1b430bed-5a73-54e5-e063-6394a90a946e", "openfda": {"upc": ["0368071505467"], "unii": ["362O9ITL9D", "C1ENJ2TE6C"], "rxcui": ["1049221"], "spl_set_id": ["925f9787-3d1c-0189-e053-2a95a90a2972"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "12 TABLET in 1 BOTTLE (68071-5054-2)", "package_ndc": "68071-5054-2", "marketing_start_date": "20190912"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE (68071-5054-4)", "package_ndc": "68071-5054-4", "marketing_start_date": "20190912"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE (68071-5054-6)", "package_ndc": "68071-5054-6", "marketing_start_date": "20190912"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "68071-5054_1b430bed-5a73-54e5-e063-6394a90a946e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68071-5054", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}