Package 70518-3197-1

{"route": ["ORAL"], "spl_id": "46531248-8e59-6d3b-e063-6394a90a7c56", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312138"], "spl_set_id": ["a90cd1f1-5258-4b0e-92fd-c4cebe47772b"], "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": "100 POUCH in 1 BOX (70518-3197-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-3197-2)", "package_ndc": "70518-3197-1", "marketing_start_date": "20211007"}], "brand_name": "Oxcarbazepine", "product_id": "70518-3197_46531248-8e59-6d3b-e063-6394a90a7c56", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-3197", "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": "ANDA077802", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}