Package 70518-2253-0

{"route": ["ORAL"], "spl_id": "49ef443a-aaae-e38e-e063-6394a90a6979", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["b571ee0f-3c2a-4c55-9c2b-e00014e2ec7a"], "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 (70518-2253-0)", "package_ndc": "70518-2253-0", "marketing_start_date": "20190805"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-2253-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-2253-2)", "package_ndc": "70518-2253-1", "marketing_start_date": "20210803"}], "brand_name": "OXCARBAZEPINE", "product_id": "70518-2253_49ef443a-aaae-e38e-e063-6394a90a6979", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-2253", "generic_name": "OXCARBAZEPINE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OXCARBAZEPINE", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA078069", "marketing_category": "ANDA", "marketing_start_date": "20190805", "listing_expiration_date": "20271231"}