Sodium Thiosulfate 60267-0705
Product NDC
60267-0705- Manufacturer
- Hope Pharmaceuticals
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- February 14, 2012
- Listing Expires
- December 31, 2027
- Application
- NDA203923
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Thiosulfate | 250 mg/mL |
Packaging Options(1)
50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50)