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United States · US · US:50090-6185_e77465a3-38c4-4a3f-846d-b7a81f9978bc

Amlodipine Besylate and Benazepril Hydrochloride

In shortageOrange BookUNIISPLATC C08CA

Last synced from FDA National Drug Code directory (United States) on

Identification

ManufacturerA-S Medication Solutions
CountryUS (United States)
ATC codeC08CA
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    5009061850
    30 CAPSULE in 1 BOTTLE (50090-6185-0)
  • ndc11
    5009061851
    90 CAPSULE in 1 BOTTLE (50090-6185-1)

Annotations

UNII (FDA Substance ID)
864V2Q084H
AMLODIPINE BESYLATE
RxCUI 104416
Orange Book
A078466
ABABABABABAB
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Amlodipine Besylate; Benazepril Hydrochloride Capsule
Raw payload (JSON)
{
  "unii": {
    "unii": "864V2Q084H",
    "rxcui": "104416",
    "inchikey": "ZPBWCRDSRKPIDG-UHFFFAOYSA-N",
    "display_name": "AMLODIPINE BESYLATE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "6efc0ef6-0424-44fc-a9ea-eb30c3b83239": {
      "match": "brand_token",
      "title": "AMLODIPINE BESYLATE TABLET [NCS HEALTHCARE OF KY, LLC DBA VANGARD LABS]",
      "spl_version": "1",
      "published_date": "2026-06-01"
    }
  },
  "productid": "50090-6185_e77465a3-38c4-4a3f-846d-b7a81f9978bc",
  "productndc": "50090-6185",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "078466",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 2.5MG BASE;10MG",
        "product_no": "001",
        "approval_date": "Feb 5, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE;10MG",
        "product_no": "002",
        "approval_date": "Feb 5, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE;20MG",
        "product_no": "003",
        "approval_date": "Feb 5, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE;20MG",
        "product_no": "004",
        "approval_date": "Feb 5, 2010"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 5MG BASE;40MG",
        "product_no": "005",
        "approval_date": "Jul 5, 2011"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "EQ 10MG BASE;40MG",
        "product_no": "006",
        "approval_date": "Jul 5, 2011"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE",
  "shortage_reason": "Amlodipine Besylate; Benazepril Hydrochloride Capsule",
  "shortage_status": "current",
  "proprietary_name": "Amlodipine Besylate and Benazepril Hydrochloride",
  "active_ingred_unit": "mg/1; mg/1",
  "application_number": "ANDA078466",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Amlodipine Besylate and Benazepril Hydrochloride",
  "start_marketing_date": "20180801",
  "active_numerator_strength": "5; 20"
}

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