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United States · US · US:44567-247_eaa65075-3ed9-4a2c-9aa5-2f24a34bf5b2

Cefoxitin

Orange BookUNIISPLATC J01DC01

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

Identification

ManufacturerWG Critical Care, LLC
CountryUS (United States)
ATC codeJ01DC01
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    4456724710
    10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (44567-247-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, PHARMACY BULK PACKAGE

Annotations

UNII (FDA Substance ID)
Q68050H03T
CEFOXITIN SODIUM
RxCUI 203118
Orange Book
A065415
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "Q68050H03T",
    "rxcui": "203118",
    "inchikey": "GNWUOVJNSFPWDD-XMZRARIVSA-M",
    "display_name": "CEFOXITIN SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAVENOUS",
  "spl_meta": {
    "91ac4c14-8dd8-4efe-a462-d1c488a6184f": {
      "match": "brand_token",
      "title": "CEFOXITIN INJECTION, POWDER, FOR SOLUTION [WG CRITICAL CARE, LLC]",
      "spl_version": "7",
      "published_date": "2025-11-17"
    }
  },
  "productid": "44567-247_eaa65075-3ed9-4a2c-9aa5-2f24a34bf5b2",
  "productndc": "44567-247",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "065415",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 10GM BASE/VIAL",
        "product_no": "001",
        "approval_date": "May 19, 2010"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CEFOXITIN SODIUM",
  "proprietary_name": "Cefoxitin",
  "active_ingred_unit": "g/1",
  "application_number": "ANDA065415",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cefoxitin",
  "start_marketing_date": "20131001",
  "active_numerator_strength": "10"
}

Related drugs

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