Package 80425-0434-1

{"route": ["ORAL"], "spl_id": "20b0177a-a97a-8703-e063-6294a90a433c", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["20aff9dc-98a7-6061-e063-6394a90a2aab"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0434-1)", "package_ndc": "80425-0434-1", "marketing_start_date": "20240827"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0434-2)", "package_ndc": "80425-0434-2", "marketing_start_date": "20240827"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0434-3)", "package_ndc": "80425-0434-3", "marketing_start_date": "20240827"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "80425-0434_20b0177a-a97a-8703-e063-6294a90a433c", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "80425-0434", "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": "50 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20240827", "listing_expiration_date": "20261231"}