Composition
- Active ingredients
- SODIUM NITRITE 300MG/10ML(30MG/ML),N/A; SODIUM THIOSULFATE N/A,12.5GM/50ML(250MG/ML)
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA201444.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Nithiodote
- Active substance
- sodium nitrite
- Route
- Intravenous
- Dosage form
- Solution, solution
- Applicant
- Hope Pharms
- Status
- Prescription
- FDA approval
- 14 Jan 2011
- Application
- NDA201444-001