Package 66267-106-30

{"route": ["ORAL"], "spl_id": "1f98dacb-a43f-a029-e063-6294a90a7609", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0366267106917"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["3e35fb03-9173-6731-e054-00144ff8d46c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (66267-106-30)", "package_ndc": "66267-106-30", "marketing_start_date": "20161006"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (66267-106-60)", "package_ndc": "66267-106-60", "marketing_start_date": "20161006"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (66267-106-90)", "package_ndc": "66267-106-90", "marketing_start_date": "20161006"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (66267-106-91)", "package_ndc": "66267-106-91", "marketing_start_date": "20161006"}], "brand_name": "Hydrochlorothiazide", "product_id": "66267-106_1f98dacb-a43f-a029-e063-6294a90a7609", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "66267-106", "generic_name": "Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA202556", "marketing_category": "ANDA", "marketing_start_date": "20130410", "listing_expiration_date": "20261231"}