benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 40 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-320
Product ID 71205-320_63cc7078-2579-49df-8a10-8d5b3b8c169b
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 71205320
Hyphenated Format 71205-320

Supplemental Identifiers

RxCUI
898719
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 ANDA078212 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)
source: ndc

Packages (3)

71205-320-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30) 71205-320-60 60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60) 71205-320-90 90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)

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": "63cc7078-2579-49df-8a10-8d5b3b8c169b", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898719"], "spl_set_id": ["92a26516-3d84-4d7a-a770-523926507887"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)", "package_ndc": "71205-320-30", "marketing_start_date": "20190901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)", "package_ndc": "71205-320-60", "marketing_start_date": "20190901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)", "package_ndc": "71205-320-90", "marketing_start_date": "20190901"}], "brand_name": "Benazepril Hydrochloride", "product_id": "71205-320_63cc7078-2579-49df-8a10-8d5b3b8c169b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "71205-320", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20080522", "listing_expiration_date": "20261231"}