{
  "schema_version": "0.1.0",
  "id": "fda-drug-shortage:sterile-water-injection",
  "slug": "sterile-water-injection",
  "title": "FDA shortage status: Sterile Water Injection",
  "ingredient": "Sterile Water Injection",
  "status": "current",
  "source_statuses": [
    "Current"
  ],
  "brand_names": [
    "BACTERIOSTATIC WATER",
    "STERILE WATER"
  ],
  "therapeutic_categories": [
    "Other"
  ],
  "dosage_forms": [
    "Injection"
  ],
  "routes": [
    "INTRAMUSCULAR",
    "INTRAVENOUS",
    "SUBCUTANEOUS"
  ],
  "package_count": 12,
  "packages": [
    {
      "package_ndc": "63323-185-10",
      "product_ndc": "63323-185",
      "company_name": "Fresenius Kabi USA, LLC",
      "manufacturer_name": "Fresenius Kabi USA, LLC",
      "presentation": "Sterile Water For Injection In Plastic Container, Injection, 1 mL/1 mL (NDC 63323-185-10)",
      "availability": "Unavailable",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "63323-185-20",
      "product_ndc": "63323-185",
      "company_name": "Fresenius Kabi USA, LLC",
      "manufacturer_name": "Fresenius Kabi USA, LLC",
      "presentation": "Sterile Water For Injection In Plastic Container, Injection, 1 mL/1 mL (NDC 63323-185-20)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "63323-185-50",
      "product_ndc": "63323-185",
      "company_name": "Fresenius Kabi USA, LLC",
      "manufacturer_name": "Fresenius Kabi USA, LLC",
      "presentation": "Sterile Water For Injection In Plastic Container, Injection, 1 mL/1 mL (NDC 63323-185-50)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "63323-178-76",
      "product_ndc": "63323-178",
      "company_name": "Fresenius Kabi USA, LLC",
      "manufacturer_name": "Fresenius Kabi USA, LLC",
      "presentation": "Sterile Water, Injection, 1000 mL/1000 mL (NDC 63323-178-76)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAVENOUS"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0641-6147-10",
      "product_ndc": "0641-6147",
      "company_name": "Hikma Pharmaceuticals USA, Inc.",
      "manufacturer_name": "Hikma Pharmaceuticals USA Inc.",
      "presentation": "Sterile Water, Injection, 1 mL/1 mL (NDC 0641-6147-10)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/13/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0409-3977-03",
      "product_ndc": "0409-1093",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Hospira, Inc.",
      "presentation": "Bacteriostatic Water For Injection In Plastic Container, Injection, 1 mL/1 mL (NDC 0409-3977-03)",
      "availability": "Limited Availability",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/07/2026",
      "initial_posting_date": "12/03/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0409-4887-10",
      "product_ndc": "0409-4887",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Hospira, Inc.",
      "presentation": "Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-10)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/07/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0409-4887-20",
      "product_ndc": "0409-4887",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Hospira, Inc.",
      "presentation": "Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-20)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/07/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0409-4887-50",
      "product_ndc": "0409-4887",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Hospira, Inc.",
      "presentation": "Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-50)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/07/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0409-4887-99",
      "product_ndc": "0409-4887",
      "company_name": "Hospira, Inc., a Pfizer Company",
      "manufacturer_name": "Hospira, Inc.",
      "presentation": "Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-99)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/07/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "64253-020-30",
      "product_ndc": "64253-020",
      "company_name": "Medefil, Inc.",
      "manufacturer_name": "Medefil, Inc.",
      "presentation": "Sterile Water, Injection, 10 mL/10 mL (NDC 64253-020-30)",
      "availability": "Available",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/17/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    },
    {
      "package_ndc": "0487-6105-01",
      "product_ndc": "0487-6105",
      "company_name": "Nephron Pharmaceuticals Corporation",
      "manufacturer_name": "Nephron Pharmaceuticals Corporation",
      "presentation": "Sterile Water, Injection, 1 mL/1 mL (NDC 0487-6105-01)",
      "availability": "Limited Availability",
      "dosage_form": "Injection",
      "routes": [
        "INTRAMUSCULAR",
        "INTRAVENOUS",
        "SUBCUTANEOUS"
      ],
      "update_date": "08/04/2026",
      "initial_posting_date": "11/23/2021",
      "source_url": "https://api.fda.gov/drug/shortages.json"
    }
  ],
  "availability_counts": {
    "Available": 9,
    "Limited Availability": 2,
    "Unavailable": 1
  },
  "initial_posting_date": "11/23/2021",
  "latest_source_update": "08/17/2026",
  "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."
  }
}