Drug application
KENALOG (TRIAMCINOLONE ACETONIDE)
Drugs@FDA NDA 012104 · SUN PHARM INDS INC
Key facts
| Drug name | KENALOG |
|---|---|
| Active ingredients | TRIAMCINOLONE ACETONIDE |
| Application type | NDA |
| Application number | 012104 |
| Company | SUN PHARM INDS INC |
| Dosage forms | SPRAY, TOPICAL |
| Strength | 0.147MG/GM **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| TE codes | AT |
| Reference listed drug | Yes |
| Latest submission class | Type 3 - New Dosage Form |
| Latest submission status date | Oct 11, 1974 |
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: