Package 59746-337-90
Brand: losartan potassium and hydrochlorothiazide
Generic: losartan potassium and hydrochlorothiazidePackage Facts
Identity
Package NDC
59746-337-90
Digits Only
5974633790
Product NDC
59746-337
Description
90 TABLET, FILM COATED in 1 BOTTLE (59746-337-90)
Marketing
Marketing Status
Brand
losartan potassium and hydrochlorothiazide
Generic
losartan potassium and hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5357e5cd-0f2e-4296-8879-72e700f87d46", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0359746338107", "0359746337100", "0359746339104"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["e0b74a86-3d36-1af0-e538-41b45b8d2cc3"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Jubilant Cadista Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59746-337-01)", "package_ndc": "59746-337-01", "marketing_start_date": "20121030"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (59746-337-10)", "package_ndc": "59746-337-10", "marketing_start_date": "20121030"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (59746-337-30)", "package_ndc": "59746-337-30", "marketing_start_date": "20121030"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (59746-337-90)", "package_ndc": "59746-337-90", "marketing_start_date": "20121030"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "59746-337_5357e5cd-0f2e-4296-8879-72e700f87d46", "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": "59746-337", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Jubilant Cadista Pharmaceuticals Inc.", "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": "ANDA201845", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}