Package 80425-0407-2

{"route": ["ORAL"], "spl_id": "1baa56ec-7eaf-dda0-e063-6394a90af453", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["1baa56e5-34d5-c8a1-e063-6394a90ae6c7"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0407-1)", "package_ndc": "80425-0407-1", "marketing_start_date": "20240624"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0407-2)", "package_ndc": "80425-0407-2", "marketing_start_date": "20240624"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0407-3)", "package_ndc": "80425-0407-3", "marketing_start_date": "20240624"}], "brand_name": "Eszopiclone", "product_id": "80425-0407_1baa56ec-7eaf-dda0-e063-6394a90af453", "dosage_form": "TABLET, FILM COATED", "product_ndc": "80425-0407", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA091166", "marketing_category": "ANDA", "marketing_start_date": "20240624", "listing_expiration_date": "20261231"}