Drug application
PALIPERIDONE PALMITATE (PALIPERIDONE PALMITATE)
Drugs@FDA ANDA 217889 · QILU
Key facts
| Drug name | PALIPERIDONE PALMITATE |
|---|---|
| Active ingredients | PALIPERIDONE PALMITATE |
| Application type | ANDA |
| Application number | 217889 |
| Company | QILU |
| Dosage forms | SUSPENSION, EXTENDED RELEASE, INJECTABLE |
| Strength | 117MG/0.75ML |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Jun 28, 2024 |
At a glance
- 1–9 Submissions
- None Label versions
- None 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.