benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: solco healthcare u.s., llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler solco healthcare u.s., llc
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 5 mg/1

Manufacturer
Solco healthcare U.S., LLC

Identifiers & Regulatory

Product NDC 43547-335
Product ID 43547-335_fc8f15d2-3382-4933-a6bb-b1c57d50d57b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076118
Listing Expiration 2026-12-31
Marketing Start 2014-01-01

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 43547335
Hyphenated Format 43547-335

Supplemental Identifiers

RxCUI
898687 898690 898719 898723
UPC
0343547338039 0343547336103 0343547336035 0343547335038 0343547337032
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 ANDA076118 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (43547-335-03)
  • 100 TABLET, COATED in 1 BOTTLE (43547-335-10)
source: ndc

Packages (2)

43547-335-03 30 TABLET, COATED in 1 BOTTLE (43547-335-03) 43547-335-10 100 TABLET, COATED in 1 BOTTLE (43547-335-10)

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": "fc8f15d2-3382-4933-a6bb-b1c57d50d57b", "openfda": {"upc": ["0343547338039", "0343547336103", "0343547336035", "0343547335038", "0343547337032"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["bb91223e-ffa5-4a3a-b191-fe121250c20c"], "manufacturer_name": ["Solco healthcare U.S., LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (43547-335-03)", "package_ndc": "43547-335-03", "marketing_start_date": "20190630"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (43547-335-10)", "package_ndc": "43547-335-10", "marketing_start_date": "20140101"}], "brand_name": "Benazepril Hydrochloride", "product_id": "43547-335_fc8f15d2-3382-4933-a6bb-b1c57d50d57b", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "43547-335", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Solco healthcare U.S., LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}