Package 68180-113-16

{"route": ["ORAL"], "spl_id": "28bc73b1-951f-459b-83ec-57aae9aafdda", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003"], "spl_set_id": ["df661166-325d-4071-9bc1-f7bf992996d2"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (68180-113-02)", "package_ndc": "68180-113-02", "marketing_start_date": "20090115"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68180-113-09)", "package_ndc": "68180-113-09", "marketing_start_date": "20090115"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (68180-113-16)", "package_ndc": "68180-113-16", "marketing_start_date": "20090115"}], "brand_name": "Levetiracetam", "product_id": "68180-113_28bc73b1-951f-459b-83ec-57aae9aafdda", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "68180-113", "generic_name": "Levetiracetam", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA078154", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}