Package 31722-193-05

{"route": ["ORAL"], "spl_id": "560e8cac-91f2-47dc-ac17-4d511598c49a", "openfda": {"upc": ["0331722194013", "0331722191012", "0331722192019"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["2a49ee34-6f1d-4ed3-8daa-343723d2a2be"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (31722-193-01)", "package_ndc": "31722-193-01", "marketing_start_date": "20170411"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (31722-193-05)", "package_ndc": "31722-193-05", "marketing_start_date": "20170411"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "31722-193_560e8cac-91f2-47dc-ac17-4d511598c49a", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "31722-193", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Camber 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": "7.5 mg/1"}], "application_number": "ANDA207419", "marketing_category": "ANDA", "marketing_start_date": "20170411", "listing_expiration_date": "20261231"}