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 · 6

ndc11
7133510861
30 TABLET in 1 BOTTLE (71335-1086-1)
ndc11
7133510862
60 TABLET in 1 BOTTLE (71335-1086-2)
ndc11
7133510863
100 TABLET in 1 BOTTLE (71335-1086-3)
ndc11
7133510864
90 TABLET in 1 BOTTLE (71335-1086-4)
ndc11
7133510865
14 TABLET in 1 BOTTLE (71335-1086-5)
ndc11
7133510866
10 TABLET in 1 BOTTLE (71335-1086-6)

Annotations

UNII (FDA Substance ID)

N1SN99T69T

BENAZEPRIL HYDROCHLORIDE

RxCUI 235758

Orange Book

A076820

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": "71335-1086_fc9d1bd9-f945-7c61-e053-6294a90a3117",
  "productndc": "71335-1086",
  "dosage_form": "TABLET",
  "orange_book": {
    "appl_no": "076820",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Feb 3, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "002",
        "approval_date": "Feb 3, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "003",
        "approval_date": "Feb 3, 2006"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "004",
        "approval_date": "Feb 3, 2006"
      }
    ],
    "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": "ANDA076820",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Benazepril Hydrochloride",
  "start_marketing_date": "20100202",
  "active_numerator_strength": "20"
}

Related drugs

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