# BUTENAFINE HYDROCHLORIDE
> **ANDA205181** · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2017-11-16
## Drug
- **FDA Application Number:** ANDA205181
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** BUTENAFINE HYDROCHLORIDE
- **Generic name:** BUTENAFINE HYDROCHLORIDE
- **Active ingredients:** BUTENAFINE HYDROCHLORIDE
- **Dosage form:** CREAM
- **Route:** TOPICAL
- **Marketing status:** Over-the-counter
- **Sponsor:** SUN PHARMA CANADA
- **Manufacturer:** TOPCO ASSOCIATES LLC
- **First approval:** 2017-11-16
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=205181)
---
*AI Analytics · CC0 1.0*