benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 5 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-749
Product ID 23155-749_c1d00e26-e74a-43a7-b418-88a61e816cfa
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076267
Listing Expiration 2026-12-31
Marketing Start 2022-08-20

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 23155749
Hyphenated Format 23155-749

Supplemental Identifiers

RxCUI
898687 898690 898719 898723
UPC
0323155749014 0323155752014 0323155751017
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 ANDA076267 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-749-01)
  • 500 TABLET in 1 BOTTLE (23155-749-05)
source: ndc

Packages (2)

23155-749-01 100 TABLET in 1 BOTTLE (23155-749-01) 23155-749-05 500 TABLET in 1 BOTTLE (23155-749-05)

Ingredients (1)

benazepril hydrochloride (5 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": "c1d00e26-e74a-43a7-b418-88a61e816cfa", "openfda": {"upc": ["0323155749014", "0323155752014", "0323155751017"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["910dac3a-728c-4f94-a514-e2b8f4680d39"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-749-01)", "package_ndc": "23155-749-01", "marketing_start_date": "20220820"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-749-05)", "package_ndc": "23155-749-05", "marketing_start_date": "20220820"}], "brand_name": "Benazepril Hydrochloride", "product_id": "23155-749_c1d00e26-e74a-43a7-b418-88a61e816cfa", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "23155-749", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076267", "marketing_category": "ANDA", "marketing_start_date": "20220820", "listing_expiration_date": "20261231"}