Package 50090-4005-1

{"route": ["ORAL"], "spl_id": "d8bc1bbb-9f8c-439b-b3b8-000fa58fdcf3", "openfda": {"unii": ["26LUD4JO9K"], "rxcui": ["856834"], "spl_set_id": ["0067b698-ee1d-4524-b1cc-af1028d13736"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4005-0)", "package_ndc": "50090-4005-0", "marketing_start_date": "20181227"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-4005-1)", "package_ndc": "50090-4005-1", "marketing_start_date": "20171226"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-4005-4)", "package_ndc": "50090-4005-4", "marketing_start_date": "20190212"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-4005-8)", "package_ndc": "50090-4005-8", "marketing_start_date": "20171226"}], "brand_name": "Amitriptyline Hydrochloride", "product_id": "50090-4005_d8bc1bbb-9f8c-439b-b3b8-000fa58fdcf3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Tricyclic Antidepressant [EPC]"], "product_ndc": "50090-4005", "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": "ANDA210086", "marketing_category": "ANDA", "marketing_start_date": "20171226", "listing_expiration_date": "20261231"}