United States · FDA National Drug Code directory
Sodium Thiosulfate
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 60267-705_4c4f587f-fb6f-4ce3-a09e-2a6a589b4d2b
- Product NDC
- 60267-705
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sodium Thiosulfate
- Labeler
- Hope Pharmaceuticals
- Marketing category
- NDA
- Marketing start / end (source format)
- 20120214
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM THIOSULFATE — 250 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50) · 60267-705-50
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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