Package 69584-885-90

{"route": ["ORAL"], "spl_id": "21124c29-b0a7-4729-90f8-0e971d265b61", "openfda": {"upc": ["0369584885909", "0369584884902"], "unii": ["6E8ZO8LRNM"], "rxcui": ["856373", "856377"], "spl_set_id": ["283c8236-9776-44cb-b7b2-1024689de736"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-10)", "package_ndc": "69584-885-10", "marketing_start_date": "20230301"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-50)", "package_ndc": "69584-885-50", "marketing_start_date": "20230301"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-90)", "package_ndc": "69584-885-90", "marketing_start_date": "20230301"}], "brand_name": "Trazodone Hydrochloride", "product_id": "69584-885_21124c29-b0a7-4729-90f8-0e971d265b61", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]"], "product_ndc": "69584-885", "generic_name": "Trazodone Hydrochloride", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trazodone Hydrochloride", "active_ingredients": [{"name": "TRAZODONE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA072193", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}