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United States · US · US:52536-340_934ec2f1-8c3f-4978-b712-33e98c4295a5

Lomustine

Orange BookUNIISPLATC L01AD02

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

Identification

ManufacturerWilshire Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeL01AD02
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    5253634005
    1 BOTTLE in 1 CARTON (52536-340-05) / 5 CAPSULE, GELATIN COATED in 1 BOTTLE

Annotations

UNII (FDA Substance ID)
7BRF0Z81KG
LOMUSTINE
RxCUI 6466
Orange Book
N017588
ABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "7BRF0Z81KG",
    "rxcui": "6466",
    "inchikey": "GQYIWUVLTXOXAJ-UHFFFAOYSA-N",
    "display_name": "LOMUSTINE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "3c3637fc-4499-4331-a3c4-6969fc86704e": {
      "match": "brand_token",
      "title": "LOMUSTINE CAPSULE, GELATIN COATED [WILSHIRE PHARMACEUTICALS, INC.]",
      "spl_version": "2",
      "published_date": "2026-04-15"
    }
  },
  "productid": "52536-340_934ec2f1-8c3f-4978-b712-33e98c4295a5",
  "productndc": "52536-340",
  "dosage_form": "CAPSULE, GELATIN COATED",
  "orange_book": {
    "appl_no": "017588",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "10MG",
        "product_no": "001",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": true,
        "rld": true,
        "te_code": "AB",
        "strength": "40MG",
        "product_no": "002",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Approved Prior to Jan 1, 1982"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": null,
        "strength": "5MG",
        "product_no": "004",
        "approval_date": "Dec 19, 2014"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "LOMUSTINE",
  "proprietary_name": "Lomustine",
  "active_ingred_unit": "mg/1",
  "application_number": "NDA017588",
  "marketing_category": "NDA",
  "nonproprietary_name": "lomustine",
  "start_marketing_date": "20260415",
  "active_numerator_strength": "10"
}

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