{
 "drug": "Azithromycin Injection",
 "asOf": "2026-08-25",
 "status": "discontinuing",
 "since": "09/09/2025",
 "dayN": 350,
 "cat": "Anti-Infective",
 "companies": [
  "Hospira, Inc., a Pfizer Company",
  "Pfizer Inc."
 ],
 "reasons": [],
 "records": [
  {
   "discontinued_date": "09/09/2025",
   "update_type": "New",
   "initial_posting_date": "09/09/2025",
   "package_ndc": "0409-0144-11",
   "generic_name": "Azithromycin Injection",
   "contact_info": "844-646-4398",
   "related_info": "Discontinuation of the manufacture of the drug",
   "update_date": "09/09/2025",
   "therapeutic_category": [
    "Anti-Infective"
   ],
   "dosage_form": "Injection",
   "presentation": "Azithromycin, Injection, 500 mg Single Dose ADD-Vantage® Glass Vial (NDC 0409-0144-11)",
   "company_name": "Hospira, Inc., a Pfizer Company",
   "status": "To Be Discontinued"
  },
  {
   "discontinued_date": "01/20/2026",
   "update_type": "New",
   "initial_posting_date": "01/20/2026",
   "package_ndc": "0069-3150-83",
   "generic_name": "Azithromycin Injection",
   "contact_info": "844-646-4398",
   "related_info": "Discontinuation of the manufacture of the drug.",
   "openfda": {
    "application_number": [
     "NDA050733"
    ],
    "brand_name": [
     "ZITHROMAX"
    ],
    "generic_name": [
     "AZITHROMYCIN DIHYDRATE"
    ],
    "manufacturer_name": [
     "Pfizer Laboratories Div Pfizer Inc"
    ],
    "product_ndc": [
     "0069-3150"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "INTRAVENOUS"
    ],
    "substance_name": [
     "AZITHROMYCIN DIHYDRATE"
    ],
    "rxcui": [
     "1668238",
     "1668240"
    ],
    "spl_id": [
     "73a19258-3cc4-49b1-8f18-e17fd418fe36"
    ],
    "spl_set_id": [
     "3b631aa1-2d46-40bc-a614-d698301ea4f9"
    ],
    "package_ndc": [
     "0069-3150-84",
     "0069-3150-83"
    ],
    "unii": [
     "5FD1131I7S"
    ]
   },
   "update_date": "01/20/2026",
   "therapeutic_category": [
    "Anti-Infective"
   ],
   "dosage_form": "Injection",
   "presentation": "Zithromax IV, Injection, 500 mg/5 mL (NDC 0069-3150-83)",
   "company_name": "Pfizer Inc.",
   "status": "To Be Discontinued"
  }
 ]
}