Package 76282-155-10

{"route": ["ORAL"], "spl_id": "3a2fd599-143e-4dc4-b22c-e08f8b16a19e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798"], "spl_set_id": ["b5a1b38c-0433-4649-a8b0-f72db0a96c45"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Exelan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76282-155-01)", "package_ndc": "76282-155-01", "marketing_start_date": "20160830"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76282-155-05)", "package_ndc": "76282-155-05", "marketing_start_date": "20160830"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76282-155-10)", "package_ndc": "76282-155-10", "marketing_start_date": "20160830"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76282-155-90)", "package_ndc": "76282-155-90", "marketing_start_date": "20160830"}], "brand_name": "Hydrochlorothiazide", "product_id": "76282-155_3a2fd599-143e-4dc4-b22c-e08f8b16a19e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "76282-155", "generic_name": "Hydrochlorothiazide", "labeler_name": "Exelan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20160830", "listing_expiration_date": "20261231"}