Package 76420-983-10

{"route": ["ORAL"], "spl_id": "d5db9e70-d7a4-462d-e053-2995a90a32be", "openfda": {"unii": ["362O9ITL9D", "9N7R477WCK"], "rxcui": ["836395"], "spl_set_id": ["52693021-f60f-43bc-9b05-43db18621346"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TABLET in 1 BOTTLE (76420-983-01)", "package_ndc": "76420-983-01", "marketing_start_date": "20220114"}, {"sample": false, "description": "2 TABLET in 1 BOTTLE (76420-983-02)", "package_ndc": "76420-983-02", "marketing_start_date": "20220114"}, {"sample": false, "description": "3 TABLET in 1 BOTTLE (76420-983-03)", "package_ndc": "76420-983-03", "marketing_start_date": "20220114"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (76420-983-10)", "package_ndc": "76420-983-10", "marketing_start_date": "20220114"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-983-30)", "package_ndc": "76420-983-30", "marketing_start_date": "20220114"}], "brand_name": "Tramadol Hydrochloride and Acetaminophen", "product_id": "76420-983_d5db9e70-d7a4-462d-e053-2995a90a32be", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76420-983", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride and Acetaminophen", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "TRAMADOL HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090485", "marketing_category": "ANDA", "marketing_start_date": "20091217", "listing_expiration_date": "20261231"}