Package 50090-7183-0

{"route": ["ORAL"], "spl_id": "b8f0f192-6383-4b21-ac0a-30ff64acd54f", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856845"], "spl_set_id": ["b793f1f8-c1f9-46f0-8156-1a4957db3a1f"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-7183-0)", "package_ndc": "50090-7183-0", "marketing_start_date": "20240618"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7183-1)", "package_ndc": "50090-7183-1", "marketing_start_date": "20240618"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7183-2)", "package_ndc": "50090-7183-2", "marketing_start_date": "20240618"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7183-5)", "package_ndc": "50090-7183-5", "marketing_start_date": "20240618"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-7183_b8f0f192-6383-4b21-ac0a-30ff64acd54f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-7183", "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": "50 mg/1"}], "application_number": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20210825", "listing_expiration_date": "20261231"}