Package 62756-184-18

{"route": ["ORAL"], "spl_id": "56aeed00-02fa-483d-b4be-45362e10f5ff", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0362756183834", "0362756185838", "0362756184831"], "unii": ["VZI5B1W380"], "rxcui": ["312136", "312137", "312138"], "spl_set_id": ["7ecd5eef-46f4-407f-9b63-ba65adb3eced"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62756-184-08)", "package_ndc": "62756-184-08", "marketing_start_date": "20071009"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62756-184-13)", "package_ndc": "62756-184-13", "marketing_start_date": "20071009"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (62756-184-18)", "package_ndc": "62756-184-18", "marketing_start_date": "20071009"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (62756-184-83)", "package_ndc": "62756-184-83", "marketing_start_date": "20071009"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62756-184-88)", "package_ndc": "62756-184-88", "marketing_start_date": "20071009"}], "brand_name": "Oxcarbazepine", "product_id": "62756-184_56aeed00-02fa-483d-b4be-45362e10f5ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "62756-184", "generic_name": "Oxcarbazepine", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/1"}], "application_number": "ANDA077794", "marketing_category": "ANDA", "marketing_start_date": "20071009", "listing_expiration_date": "20261231"}