Package 55111-531-01

{"route": ["ORAL"], "spl_id": "be502229-0e61-8481-dda9-794c93637dd7", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099625", "1099678", "1099870"], "spl_set_id": ["15f8a5be-e269-2e07-60d9-1dd7bf5f5281"], "manufacturer_name": ["Dr.Reddy's Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-01)", "package_ndc": "55111-531-01", "marketing_start_date": "20080729"}, {"sample": false, "description": "500 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-05)", "package_ndc": "55111-531-05", "marketing_start_date": "20080729"}, {"sample": false, "description": "30 TABLET, DELAYED RELEASE in 1 BOTTLE (55111-531-30)", "package_ndc": "55111-531-30", "marketing_start_date": "20080729"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-531-78)  / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (55111-531-79)", "package_ndc": "55111-531-78", "marketing_start_date": "20080729"}], "brand_name": "divalproex sodium", "product_id": "55111-531_be502229-0e61-8481-dda9-794c93637dd7", "dosage_form": "TABLET, DELAYED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55111-531", "generic_name": "divalproex sodium", "labeler_name": "Dr.Reddy's Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "divalproex sodium", "active_ingredients": [{"name": "DIVALPROEX SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA078755", "marketing_category": "ANDA", "marketing_start_date": "20080729", "listing_expiration_date": "20261231"}