lotensin hct

Generic: benazepril hydrochloride and hydrochlorothiazide

Labeler: validus pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lotensin hct
Generic Name benazepril hydrochloride and hydrochlorothiazide
Labeler validus pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 20 mg/1, hydrochlorothiazide 25 mg/1

Manufacturer
Validus Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 30698-454
Product ID 30698-454_4b9222f7-7b31-4781-e063-6394a90ab188
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA020033
Listing Expiration 2027-12-31
Marketing Start 1992-05-30

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 30698454
Hyphenated Format 30698-454

Supplemental Identifiers

RxCUI
898362 898366 898367 898371 898372 898376
UPC
0330698452011 0330698454015 0330698453018
UNII
0J48LPH2TH N1SN99T69T
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 lotensin hct (source: ndc)
Generic Name benazepril hydrochloride and hydrochlorothiazide (source: ndc)
Application Number NDA020033 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (30698-454-01)
source: ndc

Packages (1)

30698-454-01 100 TABLET in 1 BOTTLE (30698-454-01)

Ingredients (2)

benazepril hydrochloride (20 mg/1) hydrochlorothiazide (25 mg/1)

Linked Drug Pages (1)

Lotensin HCT ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4b9222f7-7b31-4781-e063-6394a90ab188", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0330698452011", "0330698454015", "0330698453018"], "unii": ["0J48LPH2TH", "N1SN99T69T"], "rxcui": ["898362", "898366", "898367", "898371", "898372", "898376"], "spl_set_id": ["94c4536f-e28e-48b1-8336-b3939917e99d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-454-01)", "package_ndc": "30698-454-01", "marketing_start_date": "19920530"}], "brand_name": "Lotensin HCT", "product_id": "30698-454_4b9222f7-7b31-4781-e063-6394a90ab188", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "30698-454", "generic_name": "benazepril hydrochloride and hydrochlorothiazide", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lotensin HCT", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "NDA020033", "marketing_category": "NDA", "marketing_start_date": "19920530", "listing_expiration_date": "20271231"}