Ceftriaxone Sodium

Orange BookUNIISPLATC J01DD04

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerHospira, Inc

CountryUS (United States)

ATC codeJ01DD04

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0409733201
10 VIAL, SINGLE-USE in 1 CARTON (0409-7332-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-7332-11)

Annotations

UNII (FDA Substance ID)

023Z5BR09K

CEFTRIAXONE SODIUM

RxCUI 203172

Orange Book

A065169

APAPAPAP

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "023Z5BR09K",
    "rxcui": "203172",
    "inchikey": "PMRZKYOXTPBIQF-MAODNAKNSA-J",
    "display_name": "CEFTRIAXONE SODIUM",
    "substance_type": "chemical",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "INTRAMUSCULAR; INTRAVENOUS",
  "spl_meta": {
    "4c5c2d3f-5038-41a1-a2fe-4dcd048dbac1": {
      "match": "brand_token",
      "title": "CEFTRIAXONE (CEFTRIAXONE SODIUM) INJECTION, SOLUTION [BAXTER HEALTHCARE COMPANY]",
      "spl_version": "26",
      "published_date": "2026-05-21"
    }
  },
  "productid": "0409-7332_cc7743b1-4e7b-446a-9ec1-cc234a8bbccf",
  "productndc": "0409-7332",
  "dosage_form": "INJECTION, POWDER, FOR SOLUTION",
  "orange_book": {
    "appl_no": "065169",
    "products": [
      {
        "rs": true,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 250MG BASE/VIAL",
        "product_no": "001",
        "approval_date": "May 9, 2005"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 500MG BASE/VIAL",
        "product_no": "002",
        "approval_date": "May 9, 2005"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 1GM BASE/VIAL",
        "product_no": "003",
        "approval_date": "May 9, 2005"
      },
      {
        "rs": true,
        "rld": false,
        "te_code": "AP",
        "strength": "EQ 2GM BASE/VIAL",
        "product_no": "004",
        "approval_date": "May 9, 2005"
      }
    ],
    "appl_type": "A"
  },
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "CEFTRIAXONE SODIUM",
  "proprietary_name": "Ceftriaxone Sodium",
  "active_ingred_unit": "g/1",
  "application_number": "ANDA065169",
  "marketing_category": "ANDA",
  "nonproprietary_name": "Ceftriaxone Sodium",
  "start_marketing_date": "20050509",
  "active_numerator_strength": "1"
}

Related drugs

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