Drug application
CELONTIN (METHSUXIMIDE)
Drugs@FDA NDA 010596 · PARKE DAVIS
Key facts
| Drug name | CELONTIN |
|---|---|
| Active ingredients | METHSUXIMIDE |
| Application type | NDA |
| Application number | 010596 |
| Company | PARKE DAVIS |
| Dosage forms | CAPSULE, ORAL |
| Strength | 150MG |
| Marketing status | Discontinued |
| Reference listed drug | Yes |
| Latest submission class | Type 1 - New Molecular Entity |
| Latest submission status date | Feb 8, 1957 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 1–9 Label versions
- 1–9 Products
- None Therapeutic equivalents
- No FDA letters on file
- No 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: