Drug application
KLOTRIX (POTASSIUM CHLORIDE)
Drugs@FDA NDA 017850 · APOTHECON
Key facts
| Drug name | KLOTRIX |
|---|---|
| Active ingredients | POTASSIUM CHLORIDE |
| Application type | NDA |
| Application number | 017850 |
| Company | APOTHECON |
| Dosage forms | TABLET, EXTENDED RELEASE, ORAL |
| Strength | 10MEQ |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission class | Type 5 - New Formulation or New Manufacturer |
| Latest submission status date | May 22, 1980 |
At a glance
- 1–9 Submissions
- 10–99 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.