Package 70518-3055-6

{"route": ["ORAL"], "spl_id": "4bb9e9d5-a334-c72c-e063-6394a90a22e1", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099678"], "spl_set_id": ["5926c3ff-c995-4789-941c-d38aa7db94dc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3055-3)  / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-4)", "package_ndc": "70518-3055-3", "marketing_start_date": "20220809"}, {"sample": false, "description": "60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-5)", "package_ndc": "70518-3055-5", "marketing_start_date": "20230104"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-6)", "package_ndc": "70518-3055-6", "marketing_start_date": "20230501"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3055-7)", "package_ndc": "70518-3055-7", "marketing_start_date": "20250630"}], "brand_name": "Divalproex Sodium", "product_id": "70518-3055_4bb9e9d5-a334-c72c-e063-6394a90a22e1", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-3055", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "250 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20210323", "listing_expiration_date": "20271231"}