benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 40 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1365
Product ID 71335-1365_d05a4467-7d16-41ef-b1d4-25a4b96382f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078212
Listing Expiration 2026-12-31
Marketing Start 2008-05-22

Pharmacologic Class

Classes
angiotensin converting enzyme inhibitor [epc] angiotensin-converting enzyme inhibitors [moa] decreased blood pressure [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713351365
Hyphenated Format 71335-1365

Supplemental Identifiers

RxCUI
898719
UNII
N1SN99T69T

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 benazepril hydrochloride (source: ndc)
Generic Name benazepril hydrochloride (source: ndc)
Application Number ANDA078212 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)
source: ndc

Packages (4)

71335-1365-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1) 71335-1365-2 100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2) 71335-1365-3 60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3) 71335-1365-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)

Ingredients (1)

benazepril hydrochloride (40 mg/1)

Linked Drug Pages (1)

Benazepril Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d05a4467-7d16-41ef-b1d4-25a4b96382f2", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["58977ec4-36ea-4d81-a8f0-7298425cbc84"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1)", "package_ndc": "71335-1365-1", "marketing_start_date": "20200213"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2)", "package_ndc": "71335-1365-2", "marketing_start_date": "20191007"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3)", "package_ndc": "71335-1365-3", "marketing_start_date": "20240530"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)", "package_ndc": "71335-1365-4", "marketing_start_date": "20200311"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-1365_d05a4467-7d16-41ef-b1d4-25a4b96382f2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-1365", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}