Package 47781-230-05

{"route": ["ORAL"], "spl_id": "61dc641a-41f6-5a0e-dc3a-8a957328a9c1", "openfda": {"upc": ["0347781230012", "0347781229016", "0347781196011"], "unii": ["C1ENJ2TE6C", "362O9ITL9D"], "rxcui": ["1049214", "1049221", "1049225"], "spl_set_id": ["900ec197-720e-5428-b526-055b7756aa4a"], "manufacturer_name": ["Alvogen, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (47781-230-01)", "package_ndc": "47781-230-01", "marketing_start_date": "20120117"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (47781-230-05)", "package_ndc": "47781-230-05", "marketing_start_date": "20120117"}, {"sample": false, "description": "250 TABLET in 1 BOTTLE (47781-230-63)", "package_ndc": "47781-230-63", "marketing_start_date": "20120117"}], "brand_name": "Oxycodone and Acetaminophen", "product_id": "47781-230_61dc641a-41f6-5a0e-dc3a-8a957328a9c1", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "47781-230", "dea_schedule": "CII", "generic_name": "Oxycodone and Acetaminophen", "labeler_name": "Alvogen, 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": "ANDA202677", "marketing_category": "ANDA", "marketing_start_date": "20120117", "listing_expiration_date": "20271231"}