benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler golden state medical supply, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 40 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-465
Product ID 51407-465_30ce8132-7b6c-1c0a-e063-6394a90a224c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076118
Listing Expiration 2026-12-31
Marketing Start 2004-02-11

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 51407465
Hyphenated Format 51407-465

Supplemental Identifiers

RxCUI
898687 898690 898719 898723
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
  • 40 mg/1
source: ndc
Packaging
  • 100 TABLET, COATED in 1 BOTTLE (51407-465-01)
  • 500 TABLET, COATED in 1 BOTTLE (51407-465-05)
source: ndc

Packages (2)

51407-465-01 100 TABLET, COATED in 1 BOTTLE (51407-465-01) 51407-465-05 500 TABLET, COATED in 1 BOTTLE (51407-465-05)

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": "30ce8132-7b6c-1c0a-e063-6394a90a224c", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["cb93e793-fe4f-452c-e053-2995a90a7333"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (51407-465-01)", "package_ndc": "51407-465-01", "marketing_start_date": "20210706"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (51407-465-05)", "package_ndc": "51407-465-05", "marketing_start_date": "20210706"}], "brand_name": "Benazepril Hydrochloride", "product_id": "51407-465_30ce8132-7b6c-1c0a-e063-6394a90a224c", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "51407-465", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20040211", "listing_expiration_date": "20261231"}