Package 70518-2357-1

{"route": ["ORAL"], "spl_id": "4a04542f-f6a0-59f5-e063-6394a90ab55d", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099870"], "spl_set_id": ["0339e27d-3dbf-4c37-a14e-f53557c08e19"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-0)", "package_ndc": "70518-2357-0", "marketing_start_date": "20191010"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-2357-1)  / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2357-2)", "package_ndc": "70518-2357-1", "marketing_start_date": "20210316"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2357-5)", "package_ndc": "70518-2357-5", "marketing_start_date": "20220809"}], "brand_name": "Divalproex Sodium", "product_id": "70518-2357_4a04542f-f6a0-59f5-e063-6394a90ab55d", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-2357", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20191010", "listing_expiration_date": "20271231"}