Package 31722-539-12

{"route": ["ORAL"], "spl_id": "1735a6ea-d61a-8448-e063-6394a90a5940", "openfda": {"nui": ["N0000008486"], "upc": ["0331722539302", "0331722538305", "0331722537308", "0331722536127", "0331722539609", "0331722537124", "0331722536301"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["63b36274-89f0-42d8-9f09-f9e78e179af4"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-539-05)", "package_ndc": "31722-539-05", "marketing_start_date": "20101008"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (31722-539-12)", "package_ndc": "31722-539-12", "marketing_start_date": "20101008"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-539-30)", "package_ndc": "31722-539-30", "marketing_start_date": "20101008"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (31722-539-60)", "package_ndc": "31722-539-60", "marketing_start_date": "20101008"}], "brand_name": "Levetiracetam", "product_id": "31722-539_1735a6ea-d61a-8448-e063-6394a90a5940", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "31722-539", "generic_name": "Levetiracetam", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA090515", "marketing_category": "ANDA", "marketing_start_date": "20101008", "listing_expiration_date": "20261231"}