Package 80425-0439-1

{"route": ["ORAL"], "spl_id": "273326d2-b8f4-466a-e063-6294a90a7abb", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762", "856834"], "spl_set_id": ["19b0c015-c07f-63b7-e063-6394a90a6060"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (80425-0439-1)", "package_ndc": "80425-0439-1", "marketing_start_date": "20240524"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (80425-0439-2)", "package_ndc": "80425-0439-2", "marketing_start_date": "20240524"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0439-3)", "package_ndc": "80425-0439-3", "marketing_start_date": "20240524"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "80425-0439_273326d2-b8f4-466a-e063-6294a90a7abb", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "80425-0439", "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": "100 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20240524", "listing_expiration_date": "20261231"}