Package 65862-594-05

{"route": ["ORAL"], "spl_id": "11845a6c-59de-469b-adb0-5e00f197ab01", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563", "1099569"], "spl_set_id": ["6240cee7-6aa8-425c-ba46-f889a640f0fa"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)", "package_ndc": "65862-594-01", "marketing_start_date": "20140602"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05)", "package_ndc": "65862-594-05", "marketing_start_date": "20140602"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-594-10)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "65862-594-10", "marketing_start_date": "20140602"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-60)", "package_ndc": "65862-594-60", "marketing_start_date": "20140602"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)", "package_ndc": "65862-594-99", "marketing_start_date": "20140602"}], "brand_name": "Divalproex sodium", "product_id": "65862-594_11845a6c-59de-469b-adb0-5e00f197ab01", "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": "65862-594", "generic_name": "Divalproex sodium", "labeler_name": "Aurobindo Pharma Limited", "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"}