benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name benazepril hydrochloride
Generic Name benazepril hydrochloride
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

benazepril hydrochloride 10 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-110
Product ID 50268-110_3f7e3955-e107-517a-e063-6294a90a0b13
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA076820
Listing Expiration 2026-12-31
Marketing Start 2014-04-28

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 50268110
Hyphenated Format 50268-110

Supplemental Identifiers

RxCUI
898687 898690 898719 898723
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 ANDA076820 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 BOX (50268-110-15) / 1 TABLET in 1 BLISTER PACK (50268-110-11)
source: ndc

Packages (1)

50268-110-15 50 BLISTER PACK in 1 BOX (50268-110-15) / 1 TABLET in 1 BLISTER PACK (50268-110-11)

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": "3f7e3955-e107-517a-e063-6294a90a0b13", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687", "898690", "898719", "898723"], "spl_set_id": ["f004d7e2-fc45-8a37-e548-eeaaa327f9b5"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-110-15)  / 1 TABLET in 1 BLISTER PACK (50268-110-11)", "package_ndc": "50268-110-15", "marketing_start_date": "20140428"}], "brand_name": "Benazepril Hydrochloride", "product_id": "50268-110_3f7e3955-e107-517a-e063-6294a90a0b13", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "50268-110", "generic_name": "Benazepril Hydrochloride", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA076820", "marketing_category": "ANDA", "marketing_start_date": "20140428", "listing_expiration_date": "20261231"}