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United States · US · US:0409-2585_2d54e2f3-5269-4b4b-aac8-fc85b9d7a0b3

Cefazolin

Orange BookUNIISPLATC J01DB

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

Identification

ManufacturerHospira, Inc
CountryUS (United States)
ATC codeJ01DB
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0409258501
    25 VIAL in 1 CARTON (0409-2585-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0409-2585-11)

Annotations

UNII (FDA Substance ID)
P380M0454Z
CEFAZOLIN SODIUM
RxCUI 203171
Orange Book
A065345
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "P380M0454Z",
    "rxcui": "203171",
    "inchikey": "FLKYBGKDCCEQQM-WYUVZMMLSA-M",
    "display_name": "CEFAZOLIN SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "d91a8d13-99a0-4d87-88dc-71cbd37922b4": {
      "match": "brand_token",
      "title": "CEFAZOLIN (CEFAZOLIN SODIUM) INJECTION, SOLUTION [BAXTER HEALTHCARE CORPORATION]",
      "spl_version": "17",
      "published_date": "2026-05-21"
    }
  },
  "productid": "0409-2585_2d54e2f3-5269-4b4b-aac8-fc85b9d7a0b3",
  "productndc": "0409-2585",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "065345",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 1GM BASE/VIAL",
        "product_no": "001",
        "approval_date": "May 9, 2007"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CEFAZOLIN SODIUM",
  "proprietary_name": "Cefazolin",
  "active_ingred_unit": "g/1",
  "application_number": "ANDA065345",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cefazolin",
  "start_marketing_date": "20070509",
  "active_numerator_strength": "1"
}

Related drugs

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