FDA
Chromitope Sodium
The FDA lists this product in 2 strengths and forms.
Composition
- Active ingredients
- SODIUM CHROMATE CR-51 2mCi/VIAL
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- SODIUM CHROMATE CR-51 200uCi/ML · InjectableNDA013993-001 · Discontinued
- SODIUM CHROMATE CR-51 2mCi/VIAL · InjectableThis page
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA013993.
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
- Chromitope Sodium
- Active substance
- sodium chromate cr-51
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Bracco
- Status
- Discontinued
- FDA approval
- 27 Dec 1971
- Application
- NDA013993-002
- RxCUI
- 91510