Drug application
GRANISETRON HYDROCHLORIDE (GRANISETRON HYDROCHLORIDE)
Drugs@FDA ANDA 078090 · FRESENIUS KABI USA
Key facts
| Drug name | GRANISETRON HYDROCHLORIDE |
|---|---|
| Active ingredients | GRANISETRON HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 078090 |
| Company | FRESENIUS KABI USA |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 4MG BASE/4ML (EQ 1MG BASE/ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Jun 30, 2008 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 1–9 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: