Package 63459-201-30

{"route": ["ORAL"], "spl_id": "a505a386-c2a1-4a32-9523-b33b1528fb48", "openfda": {"nui": ["N0000175729", "N0000175651", "N0000175769"], "unii": ["R3UK8X3U3D"], "rxcui": ["205324", "213471", "226426", "260218"], "spl_set_id": ["e16c26ad-7bc2-d155-3a5d-da83ad6492c8"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]"], "pharm_class_epc": ["Sympathomimetic-like Agent [EPC]"], "manufacturer_name": ["Cephalon, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63459-201-30)", "package_ndc": "63459-201-30", "marketing_end_date": "20270831", "marketing_start_date": "20110103"}], "brand_name": "Provigil", "product_id": "63459-201_a505a386-c2a1-4a32-9523-b33b1528fb48", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic-like Agent [EPC]"], "product_ndc": "63459-201", "dea_schedule": "CIV", "generic_name": "Modafinil", "labeler_name": "Cephalon, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Provigil", "active_ingredients": [{"name": "MODAFINIL", "strength": "200 mg/1"}], "application_number": "NDA020717", "marketing_category": "NDA", "marketing_end_date": "20270831", "marketing_start_date": "19990215"}