Package 68788-4052-9

{"route": ["ORAL"], "spl_id": "15c2afe3-3309-4abc-87d1-f3eab8d89b20", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856762"], "spl_set_id": ["15c2afe3-3309-4abc-87d1-f3eab8d89b20"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-4052-3)", "package_ndc": "68788-4052-3", "marketing_start_date": "20251117"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-4052-6)", "package_ndc": "68788-4052-6", "marketing_start_date": "20251117"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (68788-4052-8)", "package_ndc": "68788-4052-8", "marketing_start_date": "20251117"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-4052-9)", "package_ndc": "68788-4052-9", "marketing_start_date": "20251117"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "68788-4052_15c2afe3-3309-4abc-87d1-f3eab8d89b20", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68788-4052", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "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": "20251117", "listing_expiration_date": "20261231"}