benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: cardinal health 107, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler cardinal health 107, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 10 mg/1

Manufacturer
Cardinal Health 107, LLC

Identifiers & Regulatory

Product NDC 55154-4343
Product ID 55154-4343_f9ad508c-0909-440b-9e04-f8402009a57e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076820
Listing Expiration 2026-12-31
Marketing Start 2014-04-28

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 551544343
Hyphenated Format 55154-4343

Supplemental Identifiers

RxCUI
898687 898690
UPC
0055154434409 0055154434300
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 ANDA076820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BAG (55154-4343-0) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

55154-4343-0 10 BLISTER PACK in 1 BAG (55154-4343-0) / 1 TABLET in 1 BLISTER PACK

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": "f9ad508c-0909-440b-9e04-f8402009a57e", "openfda": {"upc": ["0055154434409", "0055154434300"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690"], "spl_set_id": ["f265e6dd-f47e-4511-9468-282184bcd1b1"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-4343-0)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "55154-4343-0", "marketing_start_date": "20140428"}], "brand_name": "Benazepril Hydrochloride", "product_id": "55154-4343_f9ad508c-0909-440b-9e04-f8402009a57e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "55154-4343", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20140428", "listing_expiration_date": "20261231"}