FDA.reportPublic FDA data

NDC 58177-343-04 - Benazepril Hydrochloride

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
58177-343
Requested NDC
58177-343-04
Package NDCs from labels
58177-343-04, 58177-343-08
Manufacturer
ETHEX
Effective date
2007-03-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Benazepril Hydrochloride - ETHEXETHEX2007-03-28Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58177-343-04Benazepril Hydrochloride100 in 1 BOTTLETABLET, FILM COATED1001
58177-343-08Benazepril Hydrochloride500 in 1 BOTTLETABLET, FILM COATED5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58177-343BENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]12 package rows20080313_60f0fb82-d870-4f07-82af-e4aeb79ed023.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Benazepril HydrochlorideACTIVE INGREDIENTN1SN99T69TBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
BenazeprilACTIVE MOIETYUDM7Q7QWP8BENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
black iron oxideINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
carnauba waxINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
colloidal silicon dioxideINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
crospovidoneINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
FD&C Blue No. 2 aluminum lakeINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
FD&C Red No. 40 aluminum lakeINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
hypromelloseINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
lactoseINACTIVE INGREDIENTJ2B2A4N98GBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
magnesium stearateINACTIVE INGREDIENT70097M6I30BENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
microcrystalline celluloseINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
olydextroseINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
polyethylene glycolINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
starchINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
triacetinINACTIVE INGREDIENTXHX3C3X673BENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1
yellow iron oxideINACTIVE INGREDIENTBENAZEPRIL HYDROCHLORIDE (BENAZEPRIL HYDROCHLORIDE) TABLET, FILM COATED [ETHEX]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 3 · 57 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEANI Pharmaceuticals, Inc.ff732cfa-9ded-4226-b464-19c90a6865ae2026-08-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898723
rxcui: 898690
rxcui: 898687
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEAmneal Pharmaceuticals of New York LLCe0ddcfbc-c9d8-45b1-9c11-0d1eff8c1e9e2026-08-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898723
rxcui: 898690
rxcui: 898687
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEREMEDYREPACK INC.afd616b9-0c75-48be-862d-5ac18364fd9d2026-07-17Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEBryant Ranch Prepack58977ec4-36ea-4d81-a8f0-7298425cbc842026-06-05Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEPD-Rx Pharmaceuticals, Inc.5de2ea54-877d-46e9-b4c2-bf1ab9d0f19c2026-05-14Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEREMEDYREPACK INC.6dc12ab4-2282-412f-8aa1-46ec5fbbab8f2026-04-27Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDECardinal Health 107, LLCf265e6dd-f47e-4511-9468-282184bcd1b12026-04-13Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
rxcui: 898687
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEPreferred Pharmaceuticals Inc.01a3c9f6-41aa-47a7-8c56-5462c6b544162026-03-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898723
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEPreferred Pharmaceuticals, Inc.032ea0f7-3304-4778-b3a6-6125ea7537ab2026-03-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
rxcui: 898687
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEAurobindo Pharma Limited09e383a8-e912-4cf7-8fb3-05545af80dd02026-03-13Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
rxcui: 898687
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEA-S Medication Solutions7aac6a2f-85fb-4c7a-b424-9c253186dffe2026-03-03Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDEAurobindo Pharma Limited67c64de1-5579-46e4-82ee-c9bbee708e022026-01-19Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
rxcui: 898687
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLCf7f9dc46-a947-7ae3-e053-6394a90a11922026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898687
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLCfc4cd253-13ee-9424-e053-6394a90a35a82026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLCf32d01db-655b-f3d0-e053-2a95a90a04f62026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898719
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLCf99d3d0d-cee8-b260-e053-6294a90ac3cb2026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLC3631d1dc-45e1-0588-e054-00144ff88e882026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898687
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLC708110e5-fa45-44e0-9011-261f4490ea452026-01-01Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
Benazepril HydrochlorideBENAZEPRIL HYDROCHLORIDENorthwind Health Company, LLC471cd30a-401a-c8f9-e063-6294a90a47872025-12-29Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898719
LotensinBENAZEPRIL HYDROCHLORIDEValidus Pharmaceuticals LLC2abb091b-a53e-46b0-9b84-e5ee8f2bdd8e2025-09-30Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 898690
rxcui: 898687
rxcui: 898719

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.