Drug application
IRINOTECAN HYDROCHLORIDE (IRINOTECAN HYDROCHLORIDE)
Drugs@FDA ANDA 078805 · SUN PHARMA GLOBAL
Key facts
| Drug name | IRINOTECAN HYDROCHLORIDE |
|---|---|
| Active ingredients | IRINOTECAN HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 078805 |
| Company | SUN PHARMA GLOBAL |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | 40MG/2ML (20MG/ML) |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Apr 21, 2008 |
At a glance
- 1–9 Submissions
- 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.