Package 71335-0090-5

{"route": ["ORAL"], "spl_id": "acf0fa26-5b16-424b-9e49-91ee29c7e5fd", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312137"], "spl_set_id": ["38694974-3dc6-42b5-bdf9-b5354e35330b"], "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 (71335-0090-1)", "package_ndc": "71335-0090-1", "marketing_start_date": "20200604"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0090-2)", "package_ndc": "71335-0090-2", "marketing_start_date": "20200924"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0090-3)", "package_ndc": "71335-0090-3", "marketing_start_date": "20200423"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0090-4)", "package_ndc": "71335-0090-4", "marketing_start_date": "20211123"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0090-5)", "package_ndc": "71335-0090-5", "marketing_start_date": "20211123"}], "brand_name": "OXCARBAZEPINE", "product_id": "71335-0090_acf0fa26-5b16-424b-9e49-91ee29c7e5fd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-0090", "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": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20080111", "listing_expiration_date": "20261231"}