Package 68788-6452-9

{"route": ["ORAL"], "spl_id": "c9a2c3c1-56d4-4fac-8d53-877265871edd", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["24ee299f-4466-45d4-9013-17791e1998bb"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-6452-1)", "package_ndc": "68788-6452-1", "marketing_start_date": "20160805"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-6452-3)", "package_ndc": "68788-6452-3", "marketing_start_date": "20160805"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-6452-6)", "package_ndc": "68788-6452-6", "marketing_start_date": "20160805"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-6452-9)", "package_ndc": "68788-6452-9", "marketing_start_date": "20160805"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "68788-6452_c9a2c3c1-56d4-4fac-8d53-877265871edd", "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": "68788-6452", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20160805", "listing_expiration_date": "20261231"}