{
 "drug": "Fluvastatin Sodium Tablet, Extended Release",
 "asOf": "2026-08-25",
 "status": "discontinuing",
 "since": "01/27/2026",
 "dayN": 210,
 "cat": "Cardiovascular",
 "companies": [
  "Sandoz Inc."
 ],
 "reasons": [],
 "records": [
  {
   "discontinued_date": "01/27/2026",
   "update_type": "New",
   "initial_posting_date": "01/27/2026",
   "package_ndc": "0781-8017-31",
   "generic_name": "Fluvastatin Sodium Tablet, Extended Release",
   "contact_info": "800-525-8747",
   "related_info": "Discontinuation of the manufacture of the drug",
   "openfda": {
    "application_number": [
     "NDA021192"
    ],
    "brand_name": [
     "FLUVASTATIN SODIUM ER"
    ],
    "generic_name": [
     "FLUVASTATIN SODIUM"
    ],
    "manufacturer_name": [
     "Sandoz Inc"
    ],
    "product_ndc": [
     "0781-8017"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "ORAL"
    ],
    "substance_name": [
     "FLUVASTATIN SODIUM"
    ],
    "rxcui": [
     "360507"
    ],
    "spl_id": [
     "37375ca6-3a81-4d10-9b39-9aee948e51a4"
    ],
    "spl_set_id": [
     "5ab4296c-87c2-4c64-b218-d620eef51310"
    ],
    "package_ndc": [
     "0781-8017-31",
     "0781-8017-01"
    ],
    "unii": [
     "PYF7O1FV7F"
    ]
   },
   "update_date": "01/27/2026",
   "therapeutic_category": [
    "Cardiovascular"
   ],
   "dosage_form": "Tablet",
   "presentation": "Fluvastatin Sodium, Tablet, Extended Release, 80 mg (NDC 0781-8017-31)",
   "company_name": "Sandoz Inc.",
   "status": "To Be Discontinued"
  },
  {
   "discontinued_date": "01/27/2026",
   "update_type": "New",
   "initial_posting_date": "01/27/2026",
   "package_ndc": "0781-8017-01",
   "generic_name": "Fluvastatin Sodium Tablet, Extended Release",
   "contact_info": "800-525-8747",
   "related_info": "Discontinuation of the manufacture of the drug",
   "openfda": {
    "application_number": [
     "NDA021192"
    ],
    "brand_name": [
     "FLUVASTATIN SODIUM ER"
    ],
    "generic_name": [
     "FLUVASTATIN SODIUM"
    ],
    "manufacturer_name": [
     "Sandoz Inc"
    ],
    "product_ndc": [
     "0781-8017"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "ORAL"
    ],
    "substance_name": [
     "FLUVASTATIN SODIUM"
    ],
    "rxcui": [
     "360507"
    ],
    "spl_id": [
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    ],
    "spl_set_id": [
     "5ab4296c-87c2-4c64-b218-d620eef51310"
    ],
    "package_ndc": [
     "0781-8017-31",
     "0781-8017-01"
    ],
    "unii": [
     "PYF7O1FV7F"
    ]
   },
   "update_date": "01/27/2026",
   "therapeutic_category": [
    "Cardiovascular"
   ],
   "dosage_form": "Tablet",
   "presentation": "Fluvastatin Sodium, Tablet, Extended Release, 80 mg (NDC 0781-8017-01)",
   "company_name": "Sandoz Inc.",
   "status": "To Be Discontinued"
  },
  {
   "discontinued_date": "01/27/2026",
   "update_type": "New",
   "initial_posting_date": "01/27/2026",
   "package_ndc": "66758-211-31",
   "generic_name": "Fluvastatin Sodium Tablet, Extended Release",
   "contact_info": "800-525-8747",
   "related_info": "Discontinuation of the manufacture of the drug",
   "openfda": {
    "application_number": [
     "NDA021192"
    ],
    "brand_name": [
     "LESCOL XL"
    ],
    "generic_name": [
     "FLUVASTATIN SODIUM"
    ],
    "manufacturer_name": [
     "Sandoz Inc"
    ],
    "product_ndc": [
     "66758-211"
    ],
    "product_type": [
     "HUMAN PRESCRIPTION DRUG"
    ],
    "route": [
     "ORAL"
    ],
    "substance_name": [
     "FLUVASTATIN SODIUM"
    ],
    "rxcui": [
     "360507",
     "687048"
    ],
    "spl_id": [
     "726ea2db-f1b0-4b73-a515-02157db88a42"
    ],
    "spl_set_id": [
     "726ea2db-f1b0-4b73-a515-02157db88a42"
    ],
    "package_ndc": [
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     "66758-211-31"
    ],
    "unii": [
     "PYF7O1FV7F"
    ]
   },
   "update_date": "01/27/2026",
   "therapeutic_category": [
    "Cardiovascular"
   ],
   "dosage_form": "Tablet",
   "presentation": "Lescol XL, Tablet, Extended Release, 80 mg (NDC 66758-211-31)",
   "company_name": "Sandoz Inc.",
   "status": "To Be Discontinued"
  }
 ]
}