benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler amneal pharmaceuticals llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 20 mg/1

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-753
Product ID 65162-753_1897ce48-56e1-415f-9db3-224c48b3063e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076820
Listing Expiration 2026-12-31
Marketing Start 2010-02-02

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 65162753
Hyphenated Format 65162-753

Supplemental Identifiers

RxCUI
898687 898690 898719 898723
UPC
0365162751031 0365162753035 0365162754032 0365162752038
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 ANDA076820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (65162-753-03)
  • 100 TABLET in 1 BOTTLE (65162-753-10)
  • 500 TABLET in 1 BOTTLE (65162-753-50)
source: ndc

Packages (3)

65162-753-03 30 TABLET in 1 BOTTLE (65162-753-03) 65162-753-10 100 TABLET in 1 BOTTLE (65162-753-10) 65162-753-50 500 TABLET in 1 BOTTLE (65162-753-50)

Ingredients (1)

benazepril hydrochloride (20 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": "1897ce48-56e1-415f-9db3-224c48b3063e", "openfda": {"upc": ["0365162751031", "0365162753035", "0365162754032", "0365162752038"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["a216253b-27cb-42ef-b5a8-67fb05aafb88"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (65162-753-03)", "package_ndc": "65162-753-03", "marketing_start_date": "20100202"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (65162-753-10)", "package_ndc": "65162-753-10", "marketing_start_date": "20100202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65162-753-50)", "package_ndc": "65162-753-50", "marketing_start_date": "20100202"}], "brand_name": "Benazepril Hydrochloride", "product_id": "65162-753_1897ce48-56e1-415f-9db3-224c48b3063e", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "65162-753", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20100202", "listing_expiration_date": "20261231"}