Drug application
EURAX (CROTAMITON)
Drugs@FDA NDA 009112 · JOURNEY
Key facts
| Drug name | EURAX |
|---|---|
| Active ingredients | CROTAMITON |
| Application type | NDA |
| Application number | 009112 |
| Company | JOURNEY |
| Dosage forms | LOTION, TOPICAL |
| Strength | 10% |
| Marketing status | Discontinued |
| TE codes | AT |
| Reference listed drug | Yes |
| Latest submission class | Type 3 - New Dosage Form |
| Latest submission status date | Apr 29, 1955 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
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: