{
 "drug": "Diltiazem Hydrochloride Injection",
 "asOf": "2026-08-25",
 "status": "discontinuing",
 "since": "01/05/2026",
 "dayN": 232,
 "cat": "Cardiovascular",
 "companies": [
  "Hospira, Inc., a Pfizer Company"
 ],
 "reasons": [],
 "records": [
  {
   "discontinued_date": "01/05/2026",
   "update_type": "New",
   "initial_posting_date": "01/05/2026",
   "package_ndc": "0409-4350-03",
   "generic_name": "Diltiazem Hydrochloride Injection",
   "contact_info": "844-646-4398",
   "related_info": "Discontinuation of the manufacture of the drug",
   "openfda": {
    "application_number": [
     "ANDA075853"
    ],
    "brand_name": [
     "DILTIAZEM HYDROCHLORIDE"
    ],
    "generic_name": [
     "DILTIAZEM HYDROCHLORIDE"
    ],
    "manufacturer_name": [
     "Hospira, Inc."
    ],
    "product_ndc": [
     "0409-4350",
     "0409-1171"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "INTRAVENOUS"
    ],
    "substance_name": [
     "DILTIAZEM HYDROCHLORIDE"
    ],
    "rxcui": [
     "1791230",
     "1791240"
    ],
    "spl_id": [
     "9e518c0c-b7a9-457c-9ca5-6b6c132f985e"
    ],
    "spl_set_id": [
     "bba03666-ff4f-4bf6-fa92-78e1ec2d9073"
    ],
    "package_ndc": [
     "0409-1171-11",
     "0409-1171-01",
     "0409-1171-12",
     "0409-1171-02",
     "0409-4350-13",
     "0409-4350-03"
    ],
    "unii": [
     "OLH94387TE"
    ]
   },
   "update_date": "01/05/2026",
   "therapeutic_category": [
    "Cardiovascular"
   ],
   "dosage_form": "Injection",
   "presentation": "Diltiazem Hydrochloride, Injection, 100 mg Single Dose ADD-Vantage® Glass Vial (NDC 0409-4350-03)",
   "company_name": "Hospira, Inc., a Pfizer Company",
   "status": "To Be Discontinued"
  }
 ]
}