Drug application
PATHILON (TRIDIHEXETHYL CHLORIDE)
Drugs@FDA NDA 009489 · LEDERLE
Key facts
| Drug name | PATHILON |
|---|---|
| Active ingredients | TRIDIHEXETHYL CHLORIDE |
| Application type | NDA |
| Application number | 009489 |
| Company | LEDERLE |
| Dosage forms | TABLET, ORAL |
| Strength | 25MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | Sep 15, 1954 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None 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.