Package 80425-0386-3

{"route": ["ORAL"], "spl_id": "18ff1cbe-c15c-347b-e063-6394a90ae6a8", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856783"], "spl_set_id": ["18ff2901-08fd-37f0-e063-6394a90a1ad2"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0386-1)", "package_ndc": "80425-0386-1", "marketing_start_date": "20240521"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0386-2)", "package_ndc": "80425-0386-2", "marketing_start_date": "20240521"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0386-3)", "package_ndc": "80425-0386-3", "marketing_start_date": "20240521"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "80425-0386_18ff1cbe-c15c-347b-e063-6394a90ae6a8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "80425-0386", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20240521", "listing_expiration_date": "20261231"}