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United States · US · US:0121-0977_7e29cb53-c401-49b0-9b47-209601f7ec55

Cefotan

Orange BookUNIISPLATC J01DC05

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

Identification

ManufacturerPAI Holdings, LLC dba PAI Pharma
CountryUS (United States)
ATC codeJ01DC05
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0121097710
    10 VIAL in 1 TRAY (0121-0977-10) / 20 mL in 1 VIAL (0121-0977-55)

Annotations

UNII (FDA Substance ID)
0GXP746VXB
CEFOTETAN DISODIUM
RxCUI 203141
Orange Book
N050588
APAP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
  "unii": {
    "unii": "0GXP746VXB",
    "rxcui": "203141",
    "inchikey": "ZQQALMSFFARWPK-GLHLDKNHSA-L",
    "display_name": "CEFOTETAN DISODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR; INTRAVENOUS",
  "spl_meta": {
    "f1510f5e-d001-44e0-accb-27cf79fd4f9a": {
      "match": "brand_token",
      "title": "CEFOTAN (CEFOTETAN) INJECTION, POWDER, FOR SOLUTION [PAI HOLDINGS, LLC DBA PAI PHARMA]",
      "spl_version": "6",
      "published_date": "2024-04-10"
    }
  },
  "productid": "0121-0977_7e29cb53-c401-49b0-9b47-209601f7ec55",
  "productndc": "0121-0977",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "050588",
    "products": [
      {
        "rs": false,
        "rld": true,
        "te_code": "AP",
        "strength": "EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "001",
        "approval_date": "Dec 27, 1985"
      },
      {
        "rs": false,
        "rld": true,
        "te_code": "AP",
        "strength": "EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "002",
        "approval_date": "Dec 27, 1985"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 10GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**",
        "product_no": "003",
        "approval_date": "Apr 25, 1988"
      }
    ],
    "appl_type": "N"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CEFOTETAN DISODIUM",
  "proprietary_name": "Cefotan",
  "active_ingred_unit": "g/20mL",
  "application_number": "NDA050588",
  "marketing_category": "NDA",
  "nonproprietary_name": "Cefotetan",
  "start_marketing_date": "20240408",
  "active_numerator_strength": "2"
}

Related drugs

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