Package 55111-533-30

{"route": ["ORAL"], "spl_id": "bbff7587-1b4e-6616-e6f5-689bc89e1aea", "openfda": {"unii": ["644VL95AO6"], "rxcui": ["1099563"], "spl_set_id": ["2e35f833-1cf7-12eb-9567-7a191e32e138"], "manufacturer_name": ["Dr. Reddy's Laboratories Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-533-01)", "package_ndc": "55111-533-01", "marketing_start_date": "20130811"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-533-05)", "package_ndc": "55111-533-05", "marketing_start_date": "20130811"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-533-30)", "package_ndc": "55111-533-30", "marketing_start_date": "20130811"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-533-60)", "package_ndc": "55111-533-60", "marketing_start_date": "20130811"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (55111-533-78)  / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (55111-533-79)", "package_ndc": "55111-533-78", "marketing_start_date": "20130811"}], "brand_name": "Divalproex Sodium", "product_id": "55111-533_bbff7587-1b4e-6616-e6f5-689bc89e1aea", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]", "Mood Stabilizer [EPC]"], "product_ndc": "55111-533", "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": "250 mg/1"}], "application_number": "ANDA090161", "marketing_category": "ANDA", "marketing_start_date": "20130811", "listing_expiration_date": "20261231"}