benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler chartwell rx, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 5 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-719
Product ID 62135-719_24246e61-c66b-9c3e-e063-6294a90a5207
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 62135719
Hyphenated Format 62135-719

Supplemental Identifiers

RxCUI
898687 898690 898719 898723
UPC
0362135721909 0362135720902 0362135719906 0362135722906
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
  • 90 TABLET in 1 BOTTLE (62135-719-90)
source: ndc

Packages (1)

62135-719-90 90 TABLET in 1 BOTTLE (62135-719-90)

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": "24246e61-c66b-9c3e-e063-6294a90a5207", "openfda": {"upc": ["0362135721909", "0362135720902", "0362135719906", "0362135722906"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["df13d8d8-0d70-4d6f-9dd1-5da38fbe2562"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-719-90)", "package_ndc": "62135-719-90", "marketing_start_date": "20230720"}], "brand_name": "Benazepril hydrochloride", "product_id": "62135-719_24246e61-c66b-9c3e-e063-6294a90a5207", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "62135-719", "generic_name": "Benazepril hydrochloride", "labeler_name": "Chartwell RX, LLC", "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"}