# Sodium Thiosulfate

NDC: 60267-705
Generic name: Sodium Thiosulfate
Labeler / Manufacturer: Hope Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20120214

FDA application: NDA203923

## Active ingredients

- SODIUM THIOSULFATE: 250 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60267-705"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60267-705
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=82f55408-2de9-463d-85e8-b39c3b259f0b