benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: aurobindo pharma limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler aurobindo pharma limited
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 20 mg/1

Manufacturer
Aurobindo Pharma Limited

Identifiers & Regulatory

Product NDC 65862-117
Product ID 65862-117_65334c7f-e49f-44d9-a6c1-6c1ce6e88fbe
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 65862117
Hyphenated Format 65862-117

Supplemental Identifiers

RxCUI
898687 898690 898719
UPC
0365862117908 0365862118905 0365862116901
UNII
N1SN99T69T

Packaging Origin

Original Packager
true

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
  • 20 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01)
  • 90 TABLET, FILM COATED in 1 BOTTLE (65862-117-90)
source: ndc

Packages (2)

65862-117-01 100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01) 65862-117-90 90 TABLET, FILM COATED in 1 BOTTLE (65862-117-90)

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": "65334c7f-e49f-44d9-a6c1-6c1ce6e88fbe", "openfda": {"upc": ["0365862117908", "0365862118905", "0365862116901"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719"], "spl_set_id": ["09e383a8-e912-4cf7-8fb3-05545af80dd0"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01)", "package_ndc": "65862-117-01", "marketing_start_date": "20080522"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-117-90)", "package_ndc": "65862-117-90", "marketing_start_date": "20080522"}], "brand_name": "Benazepril Hydrochloride", "product_id": "65862-117_65334c7f-e49f-44d9-a6c1-6c1ce6e88fbe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "65862-117", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}