Package 70518-4465-0

{"route": ["ORAL"], "spl_id": "410a667a-7fe5-166b-e063-6294a90a730d", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312138"], "spl_set_id": ["1176d5f5-3447-4925-aed8-1a1cb4b5989d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4465-0)", "package_ndc": "70518-4465-0", "marketing_start_date": "20250904"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-4465-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-4465-2)", "package_ndc": "70518-4465-1", "marketing_start_date": "20251012"}], "brand_name": "OXCARBAZEPINE", "product_id": "70518-4465_410a667a-7fe5-166b-e063-6294a90a730d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-4465", "generic_name": "OXCARBAZEPINE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "600 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20250904", "listing_expiration_date": "20261231"}