Package 71610-030-92

{"route": ["ORAL"], "spl_id": "fd96336e-88f7-4dbe-95c3-6af522e39ff8", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["bf34dd25-abe3-4587-b481-df052f085429"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-30)", "package_ndc": "71610-030-30", "marketing_start_date": "20181112"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-60)", "package_ndc": "71610-030-60", "marketing_start_date": "20180118"}, {"sample": false, "description": "150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-75)", "package_ndc": "71610-030-75", "marketing_start_date": "20180209"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-80)", "package_ndc": "71610-030-80", "marketing_start_date": "20190710"}, {"sample": false, "description": "270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-92)", "package_ndc": "71610-030-92", "marketing_start_date": "20190710"}], "brand_name": "Divalproex Sodium", "product_id": "71610-030_fd96336e-88f7-4dbe-95c3-6af522e39ff8", "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": "71610-030", "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": "ANDA077567", "marketing_category": "ANDA", "marketing_start_date": "20090129", "listing_expiration_date": "20261231"}