Drug application
BUTENAFINE HYDROCHLORIDE (BUTENAFINE HYDROCHLORIDE)
Drugs@FDA ANDA 205181 · SUN PHARMA CANADA
Key facts
| Drug name | BUTENAFINE HYDROCHLORIDE |
|---|---|
| Active ingredients | BUTENAFINE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 205181 |
| Company | SUN PHARMA CANADA |
| Dosage forms | CREAM, TOPICAL |
| Strength | 1% |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Nov 16, 2017 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
- Yes FDA letters on file
- Yes FDA reviews on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: