Benazepril Hydrochloride

Orange BookUNIISPLATC C09AA07

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBryant Ranch Prepack

CountryUS (United States)

ATC codeC09AA07

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
7133504571
30 TABLET, COATED in 1 BOTTLE (71335-0457-1)
ndc11
7133504572
60 TABLET, COATED in 1 BOTTLE (71335-0457-2)
ndc11
7133504573
100 TABLET, COATED in 1 BOTTLE (71335-0457-3)
ndc11
7133504574
90 TABLET, COATED in 1 BOTTLE (71335-0457-4)

Annotations

UNII (FDA Substance ID)

N1SN99T69T

BENAZEPRIL HYDROCHLORIDE

RxCUI 235758

Orange Book

A076118

ABABABAB

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "N1SN99T69T",
    "rxcui": "235758",
    "inchikey": "VPSRQEHTHIMDQM-FKLPMGAJSA-N",
    "display_name": "BENAZEPRIL HYDROCHLORIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "5de2ea54-877d-46e9-b4c2-bf1ab9d0f19c": {
      "match": "brand_token",
      "title": "BENAZEPRIL HYDROCHLORIDE TABLET, FILM COATED [PD-RX PHARMACEUTICALS, INC.]",
      "spl_version": "30",
      "published_date": "2026-05-20"
    }
  },
  "productid": "71335-0457_9b7748b4-9ef6-4dbd-9589-916d87c9e991",
  "productndc": "71335-0457",
  "dosage_form": "TABLET, COATED",
  "orange_book": {
    "appl_no": "076118",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Feb 11, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Feb 11, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Feb 11, 2004"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "004",
        "approval_date": "Feb 11, 2004"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "BENAZEPRIL HYDROCHLORIDE",
  "proprietary_name": "Benazepril Hydrochloride",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA076118",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Benazepril Hydrochloride",
  "start_marketing_date": "20140101",
  "active_numerator_strength": "10"
}

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