FDA
Naftifine Hydrochloride
The FDA lists this product in 6 strengths and forms.
Composition
- Active ingredients
- NAFTIFINE HYDROCHLORIDE 2%
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NAFTIFINE HYDROCHLORIDE 2% · CreamANDA206960-001 · Discontinued
- NAFTIFINE HYDROCHLORIDE 2% · GelANDA208201-001 · Prescription
- NAFTIFINE HYDROCHLORIDE 1% · CreamANDA205975-001 · Prescription
- NAFTIFINE HYDROCHLORIDE 2% · CreamANDA210038-001 · Prescription
- NAFTIFINE HYDROCHLORIDE 2% · CreamThis page
- NAFTIFINE HYDROCHLORIDE 1% · GelANDA206165-001 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA206901.
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
- Naftifine Hydrochloride
- Route
- Topical
- Dosage form
- Cream
- Applicant
- Sun Pharma Canada
- Status
- Prescription
- FDA approval
- 6 Jan 2016
- Application
- ANDA206901-001