Package 83008-086-90
Brand: losartan potassium and hydrochlorothiazide
Generic: losartan potassium and hydrochlorothiazidePackage Facts
Identity
Package NDC
83008-086-90
Digits Only
8300808690
Product NDC
83008-086
Description
90 TABLET, FILM COATED in 1 BOTTLE (83008-086-90)
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": "b2463971-2003-4f2a-9e1b-fb50c3dd8eaa", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["a6241e63-1952-4dfa-ba94-c406059501dd"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (83008-086-90)", "package_ndc": "83008-086-90", "marketing_end_date": "20270321", "marketing_start_date": "20240828"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "83008-086_b2463971-2003-4f2a-9e1b-fb50c3dd8eaa", "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": "83008-086", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Quality Care Products, LLC", "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": "ANDA204901", "marketing_category": "ANDA", "marketing_end_date": "20270321", "marketing_start_date": "20240828"}