Drug application
KIONEX (SODIUM POLYSTYRENE SULFONATE)
Drugs@FDA ANDA 040029 · ANI PHARMS
Key facts
| Drug name | KIONEX |
|---|---|
| Active ingredients | SODIUM POLYSTYRENE SULFONATE |
| Application type | ANDA |
| Application number | 040029 |
| Company | ANI PHARMS |
| Dosage forms | POWDER, ORAL, RECTAL |
| Strength | 454GM/BOT |
| Marketing status | Prescription |
| TE codes | AA |
| Reference listed drug | No |
| Latest submission status date | Feb 6, 1998 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None 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.