Package 71335-0152-5

{"route": ["ORAL"], "spl_id": "d2184bfc-9552-47ce-a410-a259c0dbc7df", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["60f3f17d-fd28-406d-97ca-9f01f5f1c72c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0152-1)", "package_ndc": "71335-0152-1", "marketing_start_date": "20180226"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0152-2)", "package_ndc": "71335-0152-2", "marketing_start_date": "20240709"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0152-3)", "package_ndc": "71335-0152-3", "marketing_start_date": "20180410"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0152-4)", "package_ndc": "71335-0152-4", "marketing_start_date": "20240709"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-0152-5)", "package_ndc": "71335-0152-5", "marketing_start_date": "20240709"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0152-6)", "package_ndc": "71335-0152-6", "marketing_start_date": "20240709"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0152-7)", "package_ndc": "71335-0152-7", "marketing_start_date": "20240709"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-0152-8)", "package_ndc": "71335-0152-8", "marketing_start_date": "20240709"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "71335-0152_d2184bfc-9552-47ce-a410-a259c0dbc7df", "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": "71335-0152", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "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": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}