Package 68788-8363-3

{"route": ["ORAL"], "spl_id": "18c58a61-e63d-43f0-9597-47202ecf8aca", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["6f0c2fd1-0e0d-4f5f-80c4-266fcee09fa8"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8363-3)", "package_ndc": "68788-8363-3", "marketing_start_date": "20230201"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8363-6)", "package_ndc": "68788-8363-6", "marketing_start_date": "20230201"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68788-8363-8)", "package_ndc": "68788-8363-8", "marketing_start_date": "20230201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8363-9)", "package_ndc": "68788-8363-9", "marketing_start_date": "20230201"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "68788-8363_18c58a61-e63d-43f0-9597-47202ecf8aca", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "68788-8363", "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": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20271231"}