{
  "schema_version": "0.1.0",
  "id": "fda-drug-shortage:hydrocortisone-sodium-succinate-injection",
  "slug": "hydrocortisone-sodium-succinate-injection",
  "title": "FDA shortage status: Hydrocortisone Sodium Succinate Injection",
  "ingredient": "Hydrocortisone Sodium Succinate Injection",
  "status": "resolved",
  "source_statuses": [
    "Resolved"
  ],
  "brand_names": [
    "HYDROCORTISONE SODIUM SUCCINATE",
    "SOLU-CORTEF"
  ],
  "therapeutic_categories": [
    "Dermatology",
    "Endocrinology/Metabolism",
    "Gastroenterology",
    "Hematology",
    "Neurology",
    "Oncology",
    "Ophthalmology",
    "Pediatric",
    "Pulmonary/Allergy",
    "Renal",
    "Rheumatology"
  ],
  "dosage_forms": [
    "Injection"
  ],
  "routes": [
    "INTRAMUSCULAR",
    "INTRAVENOUS"
  ],
  "package_count": 8,
  "packages": [
    {
      "package_ndc": "69097-004-67",
      "product_ndc": "69097-004",
      "company_name": "Cipla Limited",
      "manufacturer_name": "Cipla USA Inc.",
      "presentation": "Hydrocortisone Sodium Succinate, Injection, 100 mg/ Vial (NDC 69097-004-67)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0011-03",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-Cortef, Injection, 100 mg/vial (NDC 0009-0011-03)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0011-04",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-cortef, Injection, 100 mg/vial (NDC 0009-0011-04)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0825-01",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-cortef, Injection, 100 mg/vial (NDC 0009-0825-01)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0005-01",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-cortef, Injection, 1000 mg/vial (NDC 0009-0005-01)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0013-05",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-cortef, Injection, 250 mg/vial (NDC 0009-0013-05)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0013-06",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-cortef, Injection, 250 mg/vial (NDC 0009-0013-06)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0009-0016-12",
      "product_ndc": "0009-0005",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Pharmacia & Upjohn Company LLC",
      "presentation": "Solu-cortef, Injection, 500 mg/vial (NDC 0009-0016-12)",
      "availability": null,
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS"
      ],
      "update_date": "02/24/2026",
      "initial_posting_date": "03/24/2023",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    }
  ],
  "availability_counts": {},
  "initial_posting_date": "03/24/2023",
  "latest_source_update": "02/24/2026",
  "source_updated_at": "2026-08-22",
  "official_url": "https://api.fda.gov/drug/shortages.json",
  "source_name": "U.S. Food and Drug Administration openFDA Drug Shortages",
  "source_license_url": "https://open.fda.gov/license/",
  "retrieved_at": "2026-08-22T15:54:11+00:00",
  "unknowns": {
    "local_availability": "Unknown. FDA status is nationwide and is not local inventory.",
    "clinical_alternatives": "Not provided. CiteFacts does not publish treatment or substitution advice.",
    "resolution_date": "Unknown unless an FDA source row provides an update date."
  },
  "derivations": {
    "status": "current when a grouped FDA row has Current; otherwise it preserves the available FDA Resolved, Discontinuation, or not-current state.",
    "ingredient_page": "Grouped by FDA generic_name, falling back to openFDA.generic_name.",
    "availability_counts": "Count of non-empty FDA package availability values; it is not a claim about local supply."
  }
}