Package 68788-8358-3

{"route": ["ORAL"], "spl_id": "0823087f-bdff-4578-b259-cc6062dfc991", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["83a77f60-ed58-4fa0-a584-e6a0c767d19d"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-3)", "package_ndc": "68788-8358-3", "marketing_start_date": "20230213"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-6)", "package_ndc": "68788-8358-6", "marketing_start_date": "20230213"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8358-9)", "package_ndc": "68788-8358-9", "marketing_start_date": "20230213"}], "brand_name": "Divalproex sodium", "product_id": "68788-8358_0823087f-bdff-4578-b259-cc6062dfc991", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "68788-8358", "generic_name": "Divalproex sodium", "labeler_name": "Preferred Pharmaceuticals, 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": "20230213", "listing_expiration_date": "20261231"}