Package 71610-205-80

{"route": ["ORAL"], "spl_id": "4a86282f-831d-4cfe-a814-19a3f544fa85", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099569"], "spl_set_id": ["177e34e9-f74d-42aa-8e3c-5fb4f41c2322"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-30)", "package_ndc": "71610-205-30", "marketing_start_date": "20181213"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-53)", "package_ndc": "71610-205-53", "marketing_start_date": "20181213"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-60)", "package_ndc": "71610-205-60", "marketing_start_date": "20181213"}, {"sample": false, "description": "120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-70)", "package_ndc": "71610-205-70", "marketing_start_date": "20181213"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-80)", "package_ndc": "71610-205-80", "marketing_start_date": "20181213"}], "brand_name": "Divalproex sodium", "product_id": "71610-205_4a86282f-831d-4cfe-a814-19a3f544fa85", "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": "71610-205", "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": "ANDA202419", "marketing_category": "ANDA", "marketing_start_date": "20140602", "listing_expiration_date": "20261231"}