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, COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0457
Product ID 71335-0457_9b7748b4-9ef6-4dbd-9589-916d87c9e991
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076118
Listing Expiration 2026-12-31
Marketing Start 2014-01-01

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 713350457
Hyphenated Format 71335-0457

Supplemental Identifiers

RxCUI
898687
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 ANDA076118 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (71335-0457-1)
  • 60 TABLET, COATED in 1 BOTTLE (71335-0457-2)
  • 100 TABLET, COATED in 1 BOTTLE (71335-0457-3)
  • 90 TABLET, COATED in 1 BOTTLE (71335-0457-4)
source: ndc

Packages (4)

71335-0457-1 30 TABLET, COATED in 1 BOTTLE (71335-0457-1) 71335-0457-2 60 TABLET, COATED in 1 BOTTLE (71335-0457-2) 71335-0457-3 100 TABLET, COATED in 1 BOTTLE (71335-0457-3) 71335-0457-4 90 TABLET, COATED in 1 BOTTLE (71335-0457-4)

Ingredients (1)

benazepril hydrochloride (10 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": "9b7748b4-9ef6-4dbd-9589-916d87c9e991", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["b0d3122a-5332-4af6-98d8-520ed70ace62"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (71335-0457-1)", "package_ndc": "71335-0457-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (71335-0457-2)", "package_ndc": "71335-0457-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (71335-0457-3)", "package_ndc": "71335-0457-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-0457-4)", "package_ndc": "71335-0457-4", "marketing_start_date": "20220209"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-0457_9b7748b4-9ef6-4dbd-9589-916d87c9e991", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-0457", "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": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}