Package 70518-3940-1

{"route": ["ORAL"], "spl_id": "3bb1f07f-7b7d-9b1f-e063-6394a90ae5e5", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["188a48ad-c412-416a-b15b-de5f232740a2"], "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 (70518-3940-0)", "package_ndc": "70518-3940-0", "marketing_start_date": "20231206"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3940-1)  / 1 TABLET, FILM COATED in 1 POUCH (70518-3940-2)", "package_ndc": "70518-3940-1", "marketing_start_date": "20240224"}], "brand_name": "Oxcarbazepine", "product_id": "70518-3940_3bb1f07f-7b7d-9b1f-e063-6394a90ae5e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "70518-3940", "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": "ANDA215939", "marketing_category": "ANDA", "marketing_start_date": "20231206", "listing_expiration_date": "20261231"}