benazepril hydrochloride

Generic: benazepril hydrochloride

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

benazepril hydrochloride 10 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-679
Product ID 43063-679_2fb065bb-3ffc-7a24-e063-6294a90a7352
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 43063679
Hyphenated Format 43063-679

Supplemental Identifiers

RxCUI
898687
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, PLASTIC (43063-679-30)
  • 90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)
source: ndc

Packages (2)

43063-679-30 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-30) 43063-679-90 90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)

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": "2fb065bb-3ffc-7a24-e063-6294a90a7352", "openfda": {"unii": ["N1SN99T69T"], "rxcui": ["898687"], "spl_set_id": ["355811f0-2885-0d49-e054-00144ff8d46c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-30)", "package_ndc": "43063-679-30", "marketing_start_date": "20160609"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-679-90)", "package_ndc": "43063-679-90", "marketing_start_date": "20240607"}], "brand_name": "Benazepril Hydrochloride", "product_id": "43063-679_2fb065bb-3ffc-7a24-e063-6294a90a7352", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]"], "product_ndc": "43063-679", "generic_name": "Benazepril Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}