lisinopril and hydrochlorothiazide
Generic: lisinopril and hydrochlorothiazide
Labeler: aurobindo pharma limitedDrug Facts
Product Profile
Brand Name
lisinopril and hydrochlorothiazide
Generic Name
lisinopril and hydrochlorothiazide
Labeler
aurobindo pharma limited
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 12.5 mg/1, lisinopril 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
65862-043
Product ID
65862-043_5e2383b2-8c0d-450f-b681-74bfb12942a7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077606
Listing Expiration
2026-12-31
Marketing Start
2006-03-14
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65862043
Hyphenated Format
65862-043
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA077606 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 12.5 mg/1
- 10 mg/1
Packaging
- 100 TABLET in 1 BOTTLE (65862-043-00)
- 100 TABLET in 1 BOTTLE (65862-043-01)
- 500 TABLET in 1 BOTTLE (65862-043-05)
- 30 TABLET in 1 BOTTLE (65862-043-30)
- 1000 TABLET in 1 BOTTLE (65862-043-99)
Packages (5)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5e2383b2-8c0d-450f-b681-74bfb12942a7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197885", "197886", "197887"], "spl_set_id": ["d7214539-6c3d-466a-a474-6fde096fa182"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-043-00)", "package_ndc": "65862-043-00", "marketing_start_date": "20060314"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-043-01)", "package_ndc": "65862-043-01", "marketing_start_date": "20060314"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65862-043-05)", "package_ndc": "65862-043-05", "marketing_start_date": "20060314"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-043-30)", "package_ndc": "65862-043-30", "marketing_start_date": "20060314"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-043-99)", "package_ndc": "65862-043-99", "marketing_start_date": "20060314"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "65862-043_5e2383b2-8c0d-450f-b681-74bfb12942a7", "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": "65862-043", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "Aurobindo Pharma Limited", "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": "ANDA077606", "marketing_category": "ANDA", "marketing_start_date": "20060314", "listing_expiration_date": "20261231"}