lisinopril and hydrochlorothiazide
Generic: lisinopril and hydrochlorothiazide
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
lisinopril and hydrochlorothiazide
Generic Name
lisinopril and hydrochlorothiazide
Labeler
proficient rx lp
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, lisinopril 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63187-467
Product ID
63187-467_41af6e44-37f8-4322-8101-9064edb4b8c1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077912
Listing Expiration
2026-12-31
Marketing Start
2006-04-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63187467
Hyphenated Format
63187-467
Supplemental Identifiers
RxCUI
UPC
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
ANDA077912 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 20 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (63187-467-00)
- 30 TABLET in 1 BOTTLE (63187-467-30)
- 60 TABLET in 1 BOTTLE (63187-467-60)
- 90 TABLET in 1 BOTTLE (63187-467-90)
Packages (4)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41af6e44-37f8-4322-8101-9064edb4b8c1", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0363187319304", "0363187467906"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197887"], "spl_set_id": ["d9895efd-fb9d-4ce9-818a-31d724b16295"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63187-467-00)", "package_ndc": "63187-467-00", "marketing_start_date": "20181101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-467-30)", "package_ndc": "63187-467-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-467-60)", "package_ndc": "63187-467-60", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-467-90)", "package_ndc": "63187-467-90", "marketing_start_date": "20181101"}], "brand_name": "LISINOPRIL AND HYDROCHLOROTHIAZIDE", "product_id": "63187-467_41af6e44-37f8-4322-8101-9064edb4b8c1", "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": "63187-467", "generic_name": "LISINOPRIL AND HYDROCHLOROTHIAZIDE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LISINOPRIL AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077912", "marketing_category": "ANDA", "marketing_start_date": "20060410", "listing_expiration_date": "20261231"}