Sodium Thiosulfate · SODIUM THIOSULFATE 250 mg/mL · Injection, Solution · Intravenous · Hope Pharmaceuticals
NDC 60267-0705-50 · 50 mL in 1 VIAL, SINGLE-DOSE · NDA · View full market →
Just 2 companies supply this market — thin enough that a single exit would be felt immediately. One of its named manufacturing plants, Curia New York, Inc., failed FDA inspectionwithin the last two years — the agency’s most serious outcome.
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No Medicare Part D plan in CMS's quarterly files lists this product. That usually means it is discontinued, a repackager's listing, or a product no plan has added to its formulary.
How Part D pricing works →No NADAC pricing on file for this NDC — NADAC covers drugs dispensed by retail community pharmacies.
Manufacturer list price as filed — not what pharmacies actually pay after discounts.
Not scored — fragility is computed for NADAC-priced NDCs.
Establishments this product's FDA label declares, located via FDA registration data. How we built this →
There's no legal definition — it meets 1 of 6 public criteria. Why that matters →
| Type | Number / code | Expires |
|---|---|---|
| patent | 8496973 | Mar 29, 2031 |
| patent | 9345724 | Jul 7, 2030 |
| patent | 10479686 | Jul 7, 2030 |
| patent | 9585912 | Jul 7, 2030 |
| patent | 11753301 | Feb 10, 2030 |
| patent | 12304813 | Feb 10, 2030 |
No FDA shortage reports for this drug or its presentations.
No enforcement reports list this package NDC.
| Labeler | Strength | First seen | Last seen |
|---|---|---|---|
| Fennec Pharmaceuticals Inc. | SODIUM THIOSULFATE 12.5 g/100mL | Jul 15, 2026 | Sep 2, 2026 |
| Hope Pharmaceuticals | SODIUM THIOSULFATE 250 mg/mL | Jul 15, 2026 | Sep 2, 2026 |
Roster from daily NDC Directory diffs — first/last seen dates start July 2026.
DrugDashboards, "Sodium Thiosulfate — NDC 60267-0705-50," retrieved September 3, 2026, https://drugdashboards.com/drug/60267070550.
Free to cite with attribution — see how the data is put together.