FdaApplication
ANDA 078262
Identifiers
- fda_app_no: ANDA078262
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2007-12-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GRANISETRON HYDROCHLORIDE | GRANISETRON HYDROCHLORIDE | EQ 0.1MG BASE/ML (EQ 0.1MG BASE/ML) | INJECTABLE;INJECTION |
1 product