Package 70518-3683-0

{"route": ["ORAL"], "spl_id": "3f283dd7-c45b-60be-e063-6294a90ac861", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625"], "spl_set_id": ["a999f402-be1d-4153-b743-cfdb95ed1562"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-0)", "package_ndc": "70518-3683-0", "marketing_start_date": "20230317"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-1)", "package_ndc": "70518-3683-1", "marketing_start_date": "20230913"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3683-2)", "package_ndc": "70518-3683-2", "marketing_start_date": "20250701"}], "brand_name": "Divalproex Sodium", "product_id": "70518-3683_3f283dd7-c45b-60be-e063-6294a90ac861", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "70518-3683", "generic_name": "Divalproex Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20230317", "listing_expiration_date": "20261231"}