Drug application
CLOZAPINE (CLOZAPINE)
Drugs@FDA ANDA 201824 · MYLAN
Key facts
| Drug name | CLOZAPINE |
|---|---|
| Active ingredients | CLOZAPINE |
| Application type | ANDA |
| Application number | 201824 |
| Company | MYLAN |
| Dosage forms | TABLET, ORALLY DISINTEGRATING, ORAL |
| Strength | 12.5MG |
| Marketing status | None (Tentative Approval) |
| Reference listed drug | No |
| Latest submission class | Not Applicable |
| Latest submission status date | Sep 15, 2015 |
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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: