Package 50090-6313-8

{"route": ["ORAL"], "spl_id": "dd76eba0-6e9a-4fb2-8185-87290c800d76", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["69c7a0bd-93d0-40fe-a6d3-f41986b802b4"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6313-0)", "package_ndc": "50090-6313-0", "marketing_start_date": "20230106"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-6313-1)", "package_ndc": "50090-6313-1", "marketing_start_date": "20230106"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-6313-4)", "package_ndc": "50090-6313-4", "marketing_start_date": "20230106"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6313-8)", "package_ndc": "50090-6313-8", "marketing_start_date": "20230106"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-6313_dd76eba0-6e9a-4fb2-8185-87290c800d76", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-6313", "generic_name": "Amitriptyline Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amitriptyline Hydrochloride", "active_ingredients": [{"name": "AMITRIPTYLINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA214548", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20261231"}