benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 10 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8877
Product ID 68788-8877_91a3d0f7-d2df-4230-ad9e-b32f7312d337
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078212
Listing Expiration 2026-12-31
Marketing Start 2025-05-19

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 687888877
Hyphenated Format 68788-8877

Supplemental Identifiers

RxCUI
898687
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
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)
  • 30 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)
  • 60 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)
  • 90 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)
source: ndc

Packages (4)

68788-8877-1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1) 68788-8877-3 30 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3) 68788-8877-6 60 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6) 68788-8877-9 90 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)

Ingredients (1)

benazepril hydrochloride (10 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": "91a3d0f7-d2df-4230-ad9e-b32f7312d337", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["91a3d0f7-d2df-4230-ad9e-b32f7312d337"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)", "package_ndc": "68788-8877-1", "marketing_start_date": "20250519"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)", "package_ndc": "68788-8877-3", "marketing_start_date": "20250519"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)", "package_ndc": "68788-8877-6", "marketing_start_date": "20250519"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)", "package_ndc": "68788-8877-9", "marketing_start_date": "20250519"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68788-8877_91a3d0f7-d2df-4230-ad9e-b32f7312d337", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68788-8877", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078212", "marketing_category": "ANDA", "marketing_start_date": "20250519", "listing_expiration_date": "20261231"}