benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler proficient rx lp
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

benazepril hydrochloride 10 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-499
Product ID 63187-499_8b462d0b-fe6e-4240-abd2-2eafbf58a98d
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 63187499
Hyphenated Format 63187-499

Supplemental Identifiers

RxCUI
898687 898723
UPC
0363187500306 0363187499907
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
  • 10 mg/1
source: ndc
Packaging
  • 30 TABLET, COATED in 1 BOTTLE (63187-499-30)
  • 60 TABLET, COATED in 1 BOTTLE (63187-499-60)
  • 90 TABLET, COATED in 1 BOTTLE (63187-499-90)
source: ndc

Packages (3)

63187-499-30 30 TABLET, COATED in 1 BOTTLE (63187-499-30) 63187-499-60 60 TABLET, COATED in 1 BOTTLE (63187-499-60) 63187-499-90 90 TABLET, COATED in 1 BOTTLE (63187-499-90)

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": "8b462d0b-fe6e-4240-abd2-2eafbf58a98d", "openfda": {"upc": ["0363187500306", "0363187499907"], "unii": ["N1SN99T69T"], "rxcui": ["898687", "898723"], "spl_set_id": ["ebdf5144-752d-456f-b46d-19cbba0bc3d7"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (63187-499-30)", "package_ndc": "63187-499-30", "marketing_start_date": "20150202"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (63187-499-60)", "package_ndc": "63187-499-60", "marketing_start_date": "20150202"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (63187-499-90)", "package_ndc": "63187-499-90", "marketing_start_date": "20150202"}], "brand_name": "Benazepril Hydrochloride", "product_id": "63187-499_8b462d0b-fe6e-4240-abd2-2eafbf58a98d", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "63187-499", "generic_name": "Benazepril Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076118", "marketing_category": "ANDA", "marketing_start_date": "20140101", "listing_expiration_date": "20261231"}