zestoretic

Generic: lisinopril and hydrochlorothiazide

Labeler: almatica pharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zestoretic
Generic Name lisinopril and hydrochlorothiazide
Labeler almatica pharma inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1

Manufacturer
Almatica Pharma Inc.

Identifiers & Regulatory

Product NDC 52427-437
Product ID 52427-437_b8a81227-c1af-6093-4d92-647ad3fee155
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019888
Listing Expiration 2026-12-31
Marketing Start 2015-04-15

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52427437
Hyphenated Format 52427-437

Supplemental Identifiers

RxCUI
197885 197886 197887 823971 823982 823986
UPC
0352427435904 0352427436901 0352427437908
UNII
0J48LPH2TH E7199S1YWR
NUI
N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name zestoretic (source: ndc)
Generic Name lisinopril and hydrochlorothiazide (source: ndc)
Application Number NDA019888 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 20 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (52427-437-90)
source: ndc

Packages (1)

52427-437-90 90 TABLET in 1 BOTTLE (52427-437-90)

Ingredients (2)

hydrochlorothiazide (25 mg/1) lisinopril (20 mg/1)

Linked Drug Pages (1)

Zestoretic ndc-match (0.9)

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 (52427-437-90)", "package_ndc": "52427-437-90", "marketing_start_date": "20150415"}], "brand_name": "Zestoretic", "product_id": "52427-437_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": "52427-437", "generic_name": "lisinopril and hydrochlorothiazide", "labeler_name": "Almatica Pharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zestoretic", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "NDA019888", "marketing_category": "NDA", "marketing_start_date": "20150415", "listing_expiration_date": "20261231"}