Package 71610-289-30

{"route": ["ORAL"], "spl_id": "214cf544-a872-5727-e063-6294a90a5843", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["9a9f5f24-e421-406f-ac91-d1f964245f54"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-30)", "package_ndc": "71610-289-30", "marketing_start_date": "20190605"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-60)", "package_ndc": "71610-289-60", "marketing_start_date": "20190605"}, {"sample": false, "description": "150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-75)", "package_ndc": "71610-289-75", "marketing_start_date": "20190605"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-80)", "package_ndc": "71610-289-80", "marketing_start_date": "20240903"}, {"sample": false, "description": "270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-92)", "package_ndc": "71610-289-92", "marketing_start_date": "20240903"}], "brand_name": "Divalproex sodium", "product_id": "71610-289_214cf544-a872-5727-e063-6294a90a5843", "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": "71610-289", "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": "250 mg/1"}], "application_number": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20140602", "listing_expiration_date": "20261231"}