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 84386-101
Product ID 84386-101_67c64de1-5579-46e4-82ee-c9bbee708e02
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078212
Listing Expiration 2027-12-31
Marketing Start 2026-01-13

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 84386101
Hyphenated Format 84386-101

Supplemental Identifiers

RxCUI
898687 898690 898719
UPC
0384386101903 0384386102900 0384386100906
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 (84386-101-01)
  • 90 TABLET, FILM COATED in 1 BOTTLE (84386-101-90)
source: ndc

Packages (2)

84386-101-01 100 TABLET, FILM COATED in 1 BOTTLE (84386-101-01) 84386-101-90 90 TABLET, FILM COATED in 1 BOTTLE (84386-101-90)

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": "67c64de1-5579-46e4-82ee-c9bbee708e02", "openfda": {"upc": ["0384386101903", "0384386102900", "0384386100906"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719"], "spl_set_id": ["67c64de1-5579-46e4-82ee-c9bbee708e02"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (84386-101-01)", "package_ndc": "84386-101-01", "marketing_start_date": "20260113"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (84386-101-90)", "package_ndc": "84386-101-90", "marketing_start_date": "20260113"}], "brand_name": "Benazepril Hydrochloride", "product_id": "84386-101_67c64de1-5579-46e4-82ee-c9bbee708e02", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "84386-101", "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": "20260113", "listing_expiration_date": "20271231"}