FDA
Nitrofurazone
The FDA lists this product in 7 strengths and forms.
Composition
- Active ingredients
- NITROFURAZONE 0.2%
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NITROFURAZONE 0.2% · OintmentANDA086077-001 · Discontinued
- NITROFURAZONE 0.2% · OintmentANDA086156-001 · Discontinued
- NITROFURAZONE 0.2% · SolutionANDA087081-001 · Discontinued
- NITROFURAZONE 0.2% · OintmentANDA084968-001 · Discontinued
- NITROFURAZONE 0.2% · OintmentANDA084393-001 · Discontinued
- NITROFURAZONE 0.2% · OintmentThis page
- NITROFURAZONE 0.2% · SolutionANDA085130-001 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA086766.
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
- Nitrofurazone
- Route
- Topical
- Dosage form
- Ointment
- Applicant
- Wendt
- Status
- Discontinued
- FDA approval
- 11 May 1981
- Application
- ANDA086766-001