Package 52427-436-90

Brand: zestoretic

Generic: lisinopril and hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 52427-436-90
Digits Only 5242743690
Product NDC 52427-436
Description

90 TABLET in 1 BOTTLE (52427-436-90)

Marketing

Marketing Status
Marketed Since 2015-04-15
Brand zestoretic
Generic lisinopril and hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b8a81227-c1af-6093-4d92-647ad3fee155", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0352427435904", "0352427436901", "0352427437908"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887", "823971", "823982", "823986"], "spl_set_id": ["0d3a966f-f937-05a8-a90f-5aa52ebbd613"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Almatica Pharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (52427-436-90)", "package_ndc": "52427-436-90", "marketing_start_date": "20150415"}], "brand_name": "Zestoretic", "product_id": "52427-436_b8a81227-c1af-6093-4d92-647ad3fee155", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "52427-436", "generic_name": "lisinopril and hydrochlorothiazide", "labeler_name": "Almatica Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zestoretic", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "NDA019888", "marketing_category": "NDA", "marketing_start_date": "20150415", "listing_expiration_date": "20261231"}