Package 72162-2142-5

{"route": ["ORAL"], "spl_id": "11e02a31-1049-4394-bbe9-6eb593aa8e00", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["56967a93-b3c0-4043-9241-585fc64e2624"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-2142-1)", "package_ndc": "72162-2142-1", "marketing_start_date": "20231012"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-2142-5)", "package_ndc": "72162-2142-5", "marketing_start_date": "20231012"}], "brand_name": "Gabapentin", "product_id": "72162-2142_11e02a31-1049-4394-bbe9-6eb593aa8e00", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72162-2142", "generic_name": "GABAPENTIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}