Benazepril Hydrochloride

Orange BookUNIISPLATC C09AA07

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

Identification

ManufacturerPreferred Pharmaceuticals Inc.

CountryUS (United States)

ATC codeC09AA07

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 4

ndc11
6878888771
100 TABLET, FILM COATED in 1 BOTTLE (68788-8877-1)
ndc11
6878888773
30 TABLET, FILM COATED in 1 BOTTLE (68788-8877-3)
ndc11
6878888776
60 TABLET, FILM COATED in 1 BOTTLE (68788-8877-6)
ndc11
6878888779
90 TABLET, FILM COATED in 1 BOTTLE (68788-8877-9)

Annotations

UNII (FDA Substance ID)

N1SN99T69T

BENAZEPRIL HYDROCHLORIDE

RxCUI 235758

Orange Book

A078212

ABABAB

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": "68788-8877_91a3d0f7-d2df-4230-ad9e-b32f7312d337",
  "productndc": "68788-8877",
  "dosage_form": "TABLET, FILM COATED",
  "orange_book": {
    "appl_no": "078212",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "May 22, 2008"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "May 22, 2008"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "003",
        "approval_date": "May 22, 2008"
      }
    ],
    "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": "ANDA078212",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Benazepril Hydrochloride",
  "start_marketing_date": "20250519",
  "active_numerator_strength": "10"
}

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