Package 70010-668-05

{"route": ["ORAL"], "spl_id": "4221a53d-0185-7219-e063-6394a90a7ff7", "openfda": {"unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["cc966d57-7cdc-4de3-bbcf-718e2fce9cb7"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70010-668-01)", "package_ndc": "70010-668-01", "marketing_start_date": "20220101"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70010-668-05)", "package_ndc": "70010-668-05", "marketing_start_date": "20220101"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "70010-668_4221a53d-0185-7219-e063-6394a90a7ff7", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "70010-668", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Granules 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": "ANDA211708", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}