Package 10702-184-10

{"route": ["ORAL"], "spl_id": "49d88f78-4902-4a91-e063-6294a90a1626", "openfda": {"nui": ["N0000175684", "N0000175690"], "upc": ["0310702185500", "0310702184107", "0310702187108", "0310702185104", "0310702186101", "0310702186507"], "unii": ["362O9ITL9D", "CD35PMG570"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["f9cf218c-af5e-4249-aa3b-a8555ed02278"], "pharm_class_epc": ["Opioid Agonist [EPC]"], "pharm_class_moa": ["Full Opioid Agonists [MoA]"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10702-184-01)", "package_ndc": "10702-184-01", "marketing_start_date": "20180209"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (10702-184-10)", "package_ndc": "10702-184-10", "marketing_start_date": "20180209"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (10702-184-50)", "package_ndc": "10702-184-50", "marketing_start_date": "20180209"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "10702-184_49d88f78-4902-4a91-e063-6294a90a1626", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "10702-184", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxycodone and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "OXYCODONE", "strength": "2.5 mg/1"}], "application_number": "ANDA210644", "marketing_category": "ANDA", "marketing_start_date": "20180209", "listing_expiration_date": "20271231"}