FDA
Sodium Iodide I 123
The FDA lists this product in 8 strengths and forms.
Composition
- Active ingredients
- SODIUM IODIDE I-123 2mCi/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- SODIUM IODIDE I-123 200uCi · CapsuleNDA018671-002 · Prescription
- SODIUM IODIDE I-123 400uCi · CapsuleNDA018671-003 · Discontinued
- SODIUM IODIDE I-123 100uCi · CapsuleNDA018671-001 · Prescription
- SODIUM IODIDE I-123 200uCi · CapsuleANDA071910-001 · Prescription
- SODIUM IODIDE I-123 200uCi · CapsuleNDA017630-003 · Discontinued
- SODIUM IODIDE I-123 100uCi · CapsuleNDA017630-001 · Discontinued
- SODIUM IODIDE I-123 2mCi/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SolutionThis page
- SODIUM IODIDE I-123 100uCi · CapsuleANDA071909-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA017630.
At a glance
- Brand name
- Sodium Iodide I 123
- Active substance
- sodium iodide i-123
- Route
- Oral
- Dosage form
- Solution
- Applicant
- Ge Healthcare
- Status
- Discontinued
- FDA approval
- 24 Mar 1976
- Application
- NDA017630-002