Package 33342-078-15

{"route": ["ORAL"], "spl_id": "a1b947a6-e356-4442-9df7-9e82b299a852", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0333342075109", "0333342074102", "0333342076106", "0333342077103"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200284", "200285", "349353", "636042", "636045"], "spl_set_id": ["771afba6-8769-4ea8-afec-358dba0aaefe"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-078-10)", "package_ndc": "33342-078-10", "marketing_start_date": "20130419"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (33342-078-15)", "package_ndc": "33342-078-15", "marketing_start_date": "20130419"}], "brand_name": "Valsartan and Hydrochlorothiazide", "product_id": "33342-078_a1b947a6-e356-4442-9df7-9e82b299a852", "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": "33342-078", "generic_name": "Valsartan and Hydrochlorothiazide", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Valsartan and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "VALSARTAN", "strength": "320 mg/1"}], "application_number": "ANDA203145", "marketing_category": "ANDA", "marketing_start_date": "20130419", "listing_expiration_date": "20261231"}