Package 55111-532-01

{"route": ["ORAL"], "spl_id": "a886188f-930f-fcf2-d361-a2a608f95154", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099596"], "spl_set_id": ["f911748c-fb3a-fe1a-ab2a-4b40455e05ef"], "manufacturer_name": ["Dr. Reddy's Laboratories Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-01)", "package_ndc": "55111-532-01", "marketing_start_date": "20090123"}, {"sample": false, "description": "500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-05)", "package_ndc": "55111-532-05", "marketing_start_date": "20090123"}, {"sample": false, "description": "30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (55111-532-30)", "package_ndc": "55111-532-30", "marketing_start_date": "20090123"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-532-78)  / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (55111-532-79)", "package_ndc": "55111-532-78", "marketing_start_date": "20090123"}], "brand_name": "Divalproex sodium", "product_id": "55111-532_a886188f-930f-fcf2-d361-a2a608f95154", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55111-532", "generic_name": "Divalproex sodium", "labeler_name": "Dr. Reddy's Laboratories Ltd", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "125 mg/1"}], "application_number": "ANDA078979", "marketing_category": "ANDA", "marketing_start_date": "20090123", "listing_expiration_date": "20261231"}