benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 5 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3324
Product ID 68071-3324_1cd70bab-30c9-fbdd-e063-6294a90a7df3
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 680713324
Hyphenated Format 68071-3324

Supplemental Identifiers

RxCUI
898723
UPC
0368071332438
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 ANDA076118 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 120 TABLET, COATED in 1 BOTTLE (68071-3324-1)
  • 30 TABLET, COATED in 1 BOTTLE (68071-3324-3)
  • 60 TABLET, COATED in 1 BOTTLE (68071-3324-6)
source: ndc

Packages (3)

68071-3324-1 120 TABLET, COATED in 1 BOTTLE (68071-3324-1) 68071-3324-3 30 TABLET, COATED in 1 BOTTLE (68071-3324-3) 68071-3324-6 60 TABLET, COATED in 1 BOTTLE (68071-3324-6)

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": "1cd70bab-30c9-fbdd-e063-6294a90a7df3", "openfda": {"upc": ["0368071332438"], "unii": ["N1SN99T69T"], "rxcui": ["898723"], "spl_set_id": ["53fea330-cc4a-3b7e-e054-00144ff88e88"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, COATED in 1 BOTTLE (68071-3324-1)", "package_ndc": "68071-3324-1", "marketing_start_date": "20170710"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (68071-3324-3)", "package_ndc": "68071-3324-3", "marketing_start_date": "20170710"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (68071-3324-6)", "package_ndc": "68071-3324-6", "marketing_start_date": "20170710"}], "brand_name": "Benazepril Hydrochloride", "product_id": "68071-3324_1cd70bab-30c9-fbdd-e063-6294a90a7df3", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "68071-3324", "generic_name": "Benazepril Hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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"}