lisinopril and hydrochlorothiazide
Generic: lisinopril and hydrochlorothiazide
Labeler: advanced rx pharmacy of tennessee, llcDrug Facts
Product Profile
Brand Name
lisinopril and hydrochlorothiazide
Generic Name
lisinopril and hydrochlorothiazide
Labeler
advanced rx pharmacy of tennessee, llc
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 12.5 mg/1, lisinopril 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
80425-0207
Product ID
80425-0207_2a99e9e8-3d1b-ee0b-e063-6294a90ae4ef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076230
Listing Expiration
2026-12-31
Marketing Start
2022-11-04
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
804250207
Hyphenated Format
80425-0207
Supplemental Identifiers
RxCUI
UNII
NUI
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
lisinopril and hydrochlorothiazide (source: ndc)
Generic Name
lisinopril and hydrochlorothiazide (source: ndc)
Application Number
ANDA076230 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
- 10 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (80425-0207-3)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a99e9e8-3d1b-ee0b-e063-6294a90ae4ef", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885"], "spl_set_id": ["ecac0280-6faa-e7f3-e053-2995a90a2bd9"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (80425-0207-3)", "package_ndc": "80425-0207-3", "marketing_start_date": "20221104"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "80425-0207_2a99e9e8-3d1b-ee0b-e063-6294a90ae4ef", "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": "80425-0207", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "10 mg/1"}], "application_number": "ANDA076230", "marketing_category": "ANDA", "marketing_start_date": "20221104", "listing_expiration_date": "20261231"}