{
 "generic_name": "Pemetrexed Disodium Injection",
 "slug": "pemetrexed-disodium-injection",
 "brand_names": [
  "Alimta",
  "Pemetrexed"
 ],
 "fda_status": [
  "To Be Discontinued"
 ],
 "last_fda_update": "10/16/2025",
 "first_posted": "10/10/2025",
 "synced_at": "2026-10-01T04:04:04.751Z",
 "presentations": [
  {
   "company": "Eli Lilly and Co.",
   "package_ndc": "0002-7640-01",
   "presentation": "Alimta, Injection, 100 mg/4 mL (NDC 0002-7640-01)",
   "availability": "Not specified",
   "availability_raw": null,
   "fda_note": "Discontinuation of the manufacture of the drug"
  },
  {
   "company": "Sandoz Inc.",
   "package_ndc": "0781-3518-76",
   "presentation": "Pemetrexed Disodium, Injection, 100 mg/4 mL (NDC 0781-3518-76)",
   "availability": "Not specified",
   "availability_raw": null,
   "fda_note": "Discontinuation of the manufacture of the drug"
  },
  {
   "company": "Eli Lilly and Co.",
   "package_ndc": "0002-7623-01",
   "presentation": "Alimta, Injection, 500 mg/20 mL (NDC 0002-7623-01)",
   "availability": "Not specified",
   "availability_raw": null,
   "fda_note": "Discontinuation of the manufacture of the drug"
  },
  {
   "company": "Sandoz Inc.",
   "package_ndc": "0781-3519-90",
   "presentation": "Pemetrexed Disodium, Injection, 500 mg/20 mL (NDC 0781-3519-90)",
   "availability": "Not specified",
   "availability_raw": null,
   "fda_note": "Discontinuation of the manufacture of the drug"
  }
 ],
 "changes": []
}