Package 71610-707-60

{"route": ["ORAL"], "spl_id": "391af5b8-2992-47ad-80dd-9b5c373f7ce4", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["0f5bb45e-836b-48ce-9764-2d50edcb202c"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-53)", "package_ndc": "71610-707-53", "marketing_start_date": "20230516"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-60)", "package_ndc": "71610-707-60", "marketing_start_date": "20230518"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-70)", "package_ndc": "71610-707-70", "marketing_start_date": "20230516"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-80)", "package_ndc": "71610-707-80", "marketing_start_date": "20230516"}], "brand_name": "Divalproex Sodium", "product_id": "71610-707_391af5b8-2992-47ad-80dd-9b5c373f7ce4", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "71610-707", "generic_name": "divalproex sodium", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex Sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA077567", "marketing_category": "ANDA", "marketing_start_date": "20090202", "listing_expiration_date": "20261231"}