Package 72865-255-05

{"route": ["ORAL"], "spl_id": "96acc27b-7400-480e-b79a-baa8ac3ab801", "openfda": {"nui": ["N0000008486"], "upc": ["0372865256909", "0372865255056", "0372865255902", "0372865256053"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["707ed63a-67ca-4a62-9cbe-cdeb5c4ab506"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72865-255-05)", "package_ndc": "72865-255-05", "marketing_start_date": "20211001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72865-255-90)", "package_ndc": "72865-255-90", "marketing_start_date": "20211001"}], "brand_name": "GABAPENTIN", "product_id": "72865-255_96acc27b-7400-480e-b79a-baa8ac3ab801", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72865-255", "generic_name": "Gabapentin", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "GABAPENTIN", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA214957", "marketing_category": "ANDA", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}