Package 43386-493-01

{"route": ["ORAL"], "spl_id": "5e566e5f-2fef-4d70-8cfe-c24b13659b8e", "openfda": {"upc": ["0343386492107", "0343386491100", "0343386491018"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["916ff456-a27e-49dc-a312-274126a8c30c"], "manufacturer_name": ["Lupin Pharmaceuticals,Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (43386-493-01)", "package_ndc": "43386-493-01", "marketing_start_date": "20170224"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43386-493-05)", "package_ndc": "43386-493-05", "marketing_start_date": "20170224"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "43386-493_5e566e5f-2fef-4d70-8cfe-c24b13659b8e", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "43386-493", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Lupin 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": "10 mg/1"}], "application_number": "ANDA204407", "marketing_category": "ANDA", "marketing_start_date": "20170224", "listing_expiration_date": "20261231"}