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United States · US · US:31722-414_24d38de8-4acf-bdac-e063-6394a90ad431

TEMOZOLOMIDE

Orange BookUNIISPLATC L01AX03

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

Identification

ManufacturerCamber Pharmaceuticals, Inc.
CountryUS (United States)
ATC codeL01AX03
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 2

  • ndc11
    3172241414
    14 CAPSULE in 1 BOTTLE (31722-414-14)
  • ndc11
    3172241431
    5 CAPSULE in 1 BOTTLE (31722-414-31)

Annotations

UNII (FDA Substance ID)
YF1K15M17Y
TEMOZOLOMIDE
RxCUI 37776
Orange Book
A210030
ABABABABABAB
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "YF1K15M17Y",
    "rxcui": "37776",
    "inchikey": "BPEGJWRSRHCHSN-UHFFFAOYSA-N",
    "display_name": "TEMOZOLOMIDE",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "28fae355-e29a-4f76-9c83-bc44663ff7d4": {
      "match": "brand_token",
      "title": "TEMOZOLOMIDE CAPSULE [OPKO PHARMACEUTICALS, LLC]",
      "spl_version": "1",
      "published_date": "2026-05-12"
    }
  },
  "productid": "31722-414_24d38de8-4acf-bdac-e063-6394a90ad431",
  "productndc": "31722-414",
  "dosage_form": "CAPSULE",
  "orange_book": {
    "appl_no": "210030",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "5MG",
        "product_no": "001",
        "approval_date": "Aug 23, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "20MG",
        "product_no": "002",
        "approval_date": "Aug 23, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "100MG",
        "product_no": "003",
        "approval_date": "Aug 23, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "140MG",
        "product_no": "004",
        "approval_date": "Aug 23, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "180MG",
        "product_no": "005",
        "approval_date": "Aug 23, 2024"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": "AB",
        "strength": "250MG",
        "product_no": "006",
        "approval_date": "Aug 23, 2024"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "TEMOZOLOMIDE",
  "proprietary_name": "TEMOZOLOMIDE",
  "active_ingred_unit": "mg/1",
  "application_number": "ANDA210030",
  "marketing_category": "ANDA",
  "nonproprietary_name": "TEMOZOLOMIDE",
  "start_marketing_date": "20240823",
  "active_numerator_strength": "140"
}

Related drugs

Other records sharing ATC code L01AX03.

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