Drug application
RHOFADE (OXYMETAZOLINE HYDROCHLORIDE)
Drugs@FDA NDA 208552 · MAYNE PHARMA
Key facts
| Drug name | RHOFADE |
|---|---|
| Active ingredients | OXYMETAZOLINE HYDROCHLORIDE |
| Application type | NDA |
| Application number | 208552 |
| Company | MAYNE PHARMA |
| Dosage forms | CREAM, TOPICAL |
| Strength | 1% |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | Yes |
| Latest submission class | Type 10 - New Indication Submitted as Distinct NDA - Not Consolidated |
| Latest submission status date | Jan 18, 2017 |
At a glance
- 1–9 Submissions
- 1–9 Label versions
- 1–9 Products
- 1–9 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: