# NAFTIFINE HYDROCHLORIDE
> **ANDA208201** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2019-04-10
## Drug
- **FDA Application Number:** ANDA208201
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** NAFTIFINE HYDROCHLORIDE
- **Generic name:** NAFTIFINE HYDROCHLORIDE
- **Active ingredients:** NAFTIFINE HYDROCHLORIDE
- **Dosage form:** GEL
- **Route:** TOPICAL
- **Marketing status:** Prescription
- **Sponsor:** SUN PHARMA CANADA
- **Manufacturer:** Sun Pharmaceutical Industries, Inc.
- **First approval:** 2019-04-10
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=208201)
---
*AI Analytics · CC0 1.0*