Package 13107-045-05

{"route": ["ORAL"], "spl_id": "c86ebd1a-f32c-4a67-9a1b-ff0a3861c124", "openfda": {"upc": ["0313107046018"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225", "1049635"], "spl_set_id": ["69df20d9-b1d5-47dc-9ff0-29987284f8c7"], "manufacturer_name": ["Aurolife Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (13107-045-01)", "package_ndc": "13107-045-01", "marketing_start_date": "20130715"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (13107-045-05)", "package_ndc": "13107-045-05", "marketing_start_date": "20130715"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (13107-045-30)", "package_ndc": "13107-045-30", "marketing_start_date": "20130715"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (13107-045-99)", "package_ndc": "13107-045-99", "marketing_start_date": "20130715"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "13107-045_c86ebd1a-f32c-4a67-9a1b-ff0a3861c124", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "13107-045", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Aurolife Pharma, LLC", "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": "ANDA201972", "marketing_category": "ANDA", "marketing_start_date": "20130715", "listing_expiration_date": "20261231"}