Package 70518-2377-0

{"route": ["ORAL"], "spl_id": "4a14ed26-97cd-9ecc-e063-6394a90a02e8", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312138"], "spl_set_id": ["54cf1343-7350-4ed7-a6cb-9230fd4b77cf"], "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 (70518-2377-0)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2377-1)", "package_ndc": "70518-2377-0", "marketing_start_date": "20191023"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-2377-2)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2377-3)", "package_ndc": "70518-2377-2", "marketing_start_date": "20210805"}], "brand_name": "OXCARBAZEPINE", "product_id": "70518-2377_4a14ed26-97cd-9ecc-e063-6394a90a02e8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2377", "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": "20191023", "listing_expiration_date": "20271231"}