Package 65862-959-01

{"route": ["ORAL"], "spl_id": "c42b86df-c94b-4e25-9ce2-737ea613374f", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["dbd47222-14f1-4588-a009-9b81b55ca60d"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01)", "package_ndc": "65862-959-01", "marketing_start_date": "20141024"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-05)", "package_ndc": "65862-959-05", "marketing_start_date": "20141024"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-959-10)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK", "package_ndc": "65862-959-10", "marketing_start_date": "20141024"}, {"sample": false, "description": "7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-71)", "package_ndc": "65862-959-71", "marketing_start_date": "20141024"}, {"sample": false, "description": "1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-99)", "package_ndc": "65862-959-99", "marketing_start_date": "20141024"}], "brand_name": "Divalproex Sodium", "product_id": "65862-959_c42b86df-c94b-4e25-9ce2-737ea613374f", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "65862-959", "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": "125 mg/1"}], "application_number": "ANDA090554", "marketing_category": "ANDA", "marketing_start_date": "20141024", "listing_expiration_date": "20261231"}