Sodium Thiosulfate 60267-0705-50

Package NDC

60267-0705-50

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

Selected Package

60267-0705-50Selected

50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50)