Package 70518-3477-0

{"route": ["ORAL"], "spl_id": "45369e96-5a20-ffba-e063-6294a90a0bbd", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["6af40b06-0a92-454c-9277-80e89de27231"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-3477-0)", "package_ndc": "70518-3477-0", "marketing_start_date": "20220816"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-3477-1)", "package_ndc": "70518-3477-1", "marketing_start_date": "20221014"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3477-3)  / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-4)", "package_ndc": "70518-3477-3", "marketing_start_date": "20230517"}, {"sample": false, "description": "100 POUCH in 1 BOX (70518-3477-5)  / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-3477-6)", "package_ndc": "70518-3477-5", "marketing_start_date": "20230823"}], "brand_name": "Divalproex sodium", "product_id": "70518-3477_45369e96-5a20-ffba-e063-6294a90a0bbd", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-3477", "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": "ANDA209286", "marketing_category": "ANDA", "marketing_start_date": "20220816", "listing_expiration_date": "20261231"}