Package 61919-484-90

{"route": ["ORAL"], "spl_id": "33efe999-f08a-baf6-e063-6294a90a54f2", "openfda": {"unii": ["362O9ITL9D", "GSL05Y1MN6"], "rxcui": ["993781"], "spl_set_id": ["8d7ca633-4448-3507-e053-2a95a90a1287"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (61919-484-90)", "package_ndc": "61919-484-90", "marketing_start_date": "20190712"}], "brand_name": "ACETAMINOPHEN AND CODEINE", "product_id": "61919-484_33efe999-f08a-baf6-e063-6294a90a54f2", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "61919-484", "dea_schedule": "CIII", "generic_name": "ACETAMINOPHEN AND CODEINE", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACETAMINOPHEN AND CODEINE", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "300 mg/1"}, {"name": "CODEINE PHOSPHATE", "strength": "30 mg/1"}], "application_number": "ANDA040419", "marketing_category": "ANDA", "marketing_start_date": "20190712", "listing_expiration_date": "20261231"}