Package 63187-918-30

{"route": ["ORAL"], "spl_id": "038d5ca0-71f9-4135-9921-2e1889a9cf23", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464"], "spl_set_id": ["33710c3c-6f17-457a-8665-04c23bca8b75"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-918-30)", "package_ndc": "63187-918-30", "marketing_start_date": "20171002"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-918-60)", "package_ndc": "63187-918-60", "marketing_start_date": "20171002"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-918-90)", "package_ndc": "63187-918-90", "marketing_start_date": "20171002"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "63187-918_038d5ca0-71f9-4135-9921-2e1889a9cf23", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "63187-918", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091617", "marketing_category": "ANDA", "marketing_start_date": "20160523", "listing_expiration_date": "20261231"}