Package 63187-394-90

{"route": ["ORAL"], "spl_id": "b2dfdcdc-96ec-4e67-8125-a35d40c42bfb", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["6dd115b5-9268-4b66-bae8-0aa2605ebbd3"], "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 (63187-394-30)", "package_ndc": "63187-394-30", "marketing_start_date": "20161003"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-394-60)", "package_ndc": "63187-394-60", "marketing_start_date": "20161003"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-394-90)", "package_ndc": "63187-394-90", "marketing_start_date": "20161003"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "63187-394_b2dfdcdc-96ec-4e67-8125-a35d40c42bfb", "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": "63187-394", "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": "50 mg/1"}], "application_number": "ANDA091617", "marketing_category": "ANDA", "marketing_start_date": "20160523", "listing_expiration_date": "20261231"}