Back to search
🇺🇸

United States · US · US:0143-9933_7e0897ec-2275-4438-9cc5-4c951e52ad97

Cefotaxime

In shortageOrange BookUNIISPLATC J01DD

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

Identification

ManufacturerHikma Pharmaceuticals USA Inc.
CountryUS (United States)
ATC codeJ01DD
Dispensing
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026

Packs · 1

  • ndc11
    0143993325
    25 VIAL in 1 PACKAGE (0143-9933-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9933-01)

Annotations

UNII (FDA Substance ID)
258J72S7TZ
CEFOTAXIME SODIUM
RxCUI 203117
Orange Book
A065072
DailyMed SPL labels
1 version tracked
FDA shortage
Currently in shortage
Cefotaxime Sodium Powder, for Solution
Raw payload (JSON)
{
  "unii": {
    "unii": "258J72S7TZ",
    "rxcui": "203117",
    "inchikey": "AZZMGZXNTDTSME-JUZDKLSSSA-M",
    "display_name": "CEFOTAXIME SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR; INTRAVENOUS",
  "spl_meta": {
    "8efe3bd0-c43a-2bd6-e053-2a95a90a92fa": {
      "match": "brand_token",
      "title": "CEFOTAXIME (CEFOTAXIME INJECTION) POWDER, FOR SOLUTION [STERIMAX INC.]",
      "spl_version": "6",
      "published_date": "2024-12-16"
    }
  },
  "productid": "0143-9933_7e0897ec-2275-4438-9cc5-4c951e52ad97",
  "productndc": "0143-9933",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "065072",
    "products": [
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 500MG BASE/VIAL",
        "product_no": "001",
        "approval_date": "Nov 20, 2002"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 1GM BASE/VIAL",
        "product_no": "002",
        "approval_date": "Nov 20, 2002"
      },
      {
        "rs": false,
        "rld": false,
        "te_code": null,
        "strength": "EQ 2GM BASE/VIAL",
        "product_no": "003",
        "approval_date": "Nov 20, 2002"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CEFOTAXIME SODIUM",
  "shortage_reason": "Cefotaxime Sodium Powder, for Solution",
  "shortage_status": "current",
  "proprietary_name": "Cefotaxime",
  "active_ingred_unit": "g/1",
  "application_number": "ANDA065072",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Cefotaxime",
  "start_marketing_date": "20021120",
  "active_numerator_strength": "2"
}

Related drugs

Other records sharing ATC code J01DD.

Access this data programmatically

Query Cefotaxime and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.