Drug application
LURASIDONE HYDROCHLORIDE (LURASIDONE HYDROCHLORIDE)
Drugs@FDA ANDA 207995 · FIRST TIME US GENERICS LLC
Key facts
| Drug name | LURASIDONE HYDROCHLORIDE |
|---|---|
| Active ingredients | LURASIDONE HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 207995 |
| Company | FIRST TIME US GENERICS LLC |
| Dosage forms | UNKNOWN |
| Strength | UNKNOWN |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission status date | Dec 12, 2018 |
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.