Drug application
GRANISETRON HYDROCHLORIDE (GRANISETRON HYDROCHLORIDE)
Drugs@FDA ANDA 079119 · EPIC PHARMA LLC
Key facts
| Drug name | GRANISETRON HYDROCHLORIDE |
|---|---|
| Active ingredients | GRANISETRON HYDROCHLORIDE |
| Application type | ANDA |
| Application number | 079119 |
| Company | EPIC PHARMA LLC |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) |
| Marketing status | Discontinued |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Sep 10, 2009 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None 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.