Package 0904-6791-04

{"route": ["ORAL"], "spl_id": "9b081f9e-c042-4aa8-833a-0701015ab9a4", "openfda": {"nui": ["N0000175729", "N0000175651", "N0000175769"], "unii": ["R3UK8X3U3D"], "rxcui": ["205324", "260218"], "spl_set_id": ["4a7ab52b-db31-4774-a06a-b11f2bb60662"], "pharm_class_pe": ["Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]"], "pharm_class_epc": ["Sympathomimetic-like Agent [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (0904-6791-04)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-6791-04", "marketing_start_date": "20140203"}], "brand_name": "Modafinil", "product_id": "0904-6791_9b081f9e-c042-4aa8-833a-0701015ab9a4", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulation [PE]", "Increased Sympathetic Activity [PE]", "Sympathomimetic-like Agent [EPC]"], "product_ndc": "0904-6791", "dea_schedule": "CIV", "generic_name": "modafinil", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Modafinil", "active_ingredients": [{"name": "MODAFINIL", "strength": "100 mg/1"}], "application_number": "ANDA077667", "marketing_category": "ANDA", "marketing_start_date": "20140203", "listing_expiration_date": "20261231"}