Active Ingredient: SODIUM NITRITE; SODIUM THIOSULFATE
Proprietary Name: NITHIODOTE
Dosage Form; Route of Administration: SOLUTION, SOLUTION; INTRAVENOUS, INTRAVENOUS
Strength: 300MG/10ML(30MG/ML),N/A;N/A,12.5GM/50ML(250MG/ML)
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N201444
Product Number: 001
Approval Date: Jan 14, 2011
Applicant Holder Full Name: HOPE PHARMACEUTICALS
Marketing Status:
Prescription
Patent and Exclusivity Information
