Package 71335-2548-4

{"route": ["ORAL"], "spl_id": "99a631d2-4db5-4d59-9d54-a6334d7b9fac", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312137"], "spl_set_id": ["23137a89-cbd0-4a5f-8220-f26b7ba54330"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2548-1)", "package_ndc": "71335-2548-1", "marketing_start_date": "20250121"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2548-2)", "package_ndc": "71335-2548-2", "marketing_start_date": "20250121"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2548-3)", "package_ndc": "71335-2548-3", "marketing_start_date": "20250121"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-2548-4)", "package_ndc": "71335-2548-4", "marketing_start_date": "20250121"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-2548-5)", "package_ndc": "71335-2548-5", "marketing_start_date": "20250121"}], "brand_name": "Oxcarbazepine", "product_id": "71335-2548_99a631d2-4db5-4d59-9d54-a6334d7b9fac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-2548", "generic_name": "Oxcarbazepine", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "300 mg/1"}], "application_number": "ANDA215939", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20261231"}