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
Routes
ORAL
Active Ingredients

benazepril hydrochloride 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-1086
Product ID 71335-1086_fc9d1bd9-f945-7c61-e053-6294a90a3117
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076820
Listing Expiration 2026-12-31
Marketing Start 2010-02-02

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 713351086
Hyphenated Format 71335-1086

Supplemental Identifiers

RxCUI
898690
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 ANDA076820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (71335-1086-1)
  • 60 TABLET in 1 BOTTLE (71335-1086-2)
  • 100 TABLET in 1 BOTTLE (71335-1086-3)
  • 90 TABLET in 1 BOTTLE (71335-1086-4)
  • 14 TABLET in 1 BOTTLE (71335-1086-5)
  • 10 TABLET in 1 BOTTLE (71335-1086-6)
source: ndc

Packages (6)

71335-1086-1 30 TABLET in 1 BOTTLE (71335-1086-1) 71335-1086-2 60 TABLET in 1 BOTTLE (71335-1086-2) 71335-1086-3 100 TABLET in 1 BOTTLE (71335-1086-3) 71335-1086-4 90 TABLET in 1 BOTTLE (71335-1086-4) 71335-1086-5 14 TABLET in 1 BOTTLE (71335-1086-5) 71335-1086-6 10 TABLET in 1 BOTTLE (71335-1086-6)

Ingredients (1)

benazepril hydrochloride (20 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": "fc9d1bd9-f945-7c61-e053-6294a90a3117", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898690"], "spl_set_id": ["2b02c240-4393-48ed-a385-561ced7b7abf"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-1086-1)", "package_ndc": "71335-1086-1", "marketing_start_date": "20220504"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-1086-2)", "package_ndc": "71335-1086-2", "marketing_start_date": "20220504"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-1086-3)", "package_ndc": "71335-1086-3", "marketing_start_date": "20220504"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-1086-4)", "package_ndc": "71335-1086-4", "marketing_start_date": "20220504"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (71335-1086-5)", "package_ndc": "71335-1086-5", "marketing_start_date": "20220504"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (71335-1086-6)", "package_ndc": "71335-1086-6", "marketing_start_date": "20220504"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71335-1086_fc9d1bd9-f945-7c61-e053-6294a90a3117", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71335-1086", "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": "20 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20100202", "listing_expiration_date": "20261231"}