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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 203923

SODIUM THIOSULFATE (SODIUM THIOSULFATE)
12.5GM/50ML (250MG/ML)
Marketing Status: Prescription
Active Ingredient: SODIUM THIOSULFATE
Proprietary Name: SODIUM THIOSULFATE
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 12.5GM/50ML (250MG/ML)
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N203923
Product Number: 001
Approval Date: Feb 14, 2012
Applicant Holder Full Name: HOPE PHARMACEUTICALS
Marketing Status:  Prescription
Patent and Exclusivity Information
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