Package 68788-8767-3

{"route": ["ORAL"], "spl_id": "f7ae98ac-21aa-41bb-bbb3-6145e02dd370", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["54485767-d7c5-4927-ae52-08537a7a91e8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8767-3)", "package_ndc": "68788-8767-3", "marketing_start_date": "20241120"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8767-6)", "package_ndc": "68788-8767-6", "marketing_start_date": "20241120"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE (68788-8767-8)", "package_ndc": "68788-8767-8", "marketing_start_date": "20241120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8767-9)", "package_ndc": "68788-8767-9", "marketing_start_date": "20241120"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "68788-8767_f7ae98ac-21aa-41bb-bbb3-6145e02dd370", "dosage_form": "TABLET", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68788-8767", "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": "50 mg/1"}], "application_number": "ANDA217411", "marketing_category": "ANDA", "marketing_start_date": "20241120", "listing_expiration_date": "20271231"}