FdaApplication
ANDA 078678
Identifiers
- fda_app_no: ANDA078678
Properties
| Property | Value |
|---|---|
| applicant_name | ORBION PHARMACEUTICALS PRIVATE LTD |
| application_type | ANDA |
| approval_date | 2008-02-13 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| GRANISETRON HYDROCHLORIDE | GRANISETRON HYDROCHLORIDE | EQ 1MG BASE | TABLET;ORAL |
1 product