FdaApplication
NDA 022110
Identifiers
- fda_app_no: NDA022110
Properties
| Property | Value |
|---|---|
| applicant_name | APOTEX INC |
| application_type | NDA |
| approval_date | 2009-09-11 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VIBATIV | TELAVANCIN HYDROCHLORIDE | EQ 750MG BASE/VIAL | POWDER;INTRAVENOUS |
| VIBATIV | TELAVANCIN HYDROCHLORIDE | EQ 250MG BASE/VIAL | POWDER;INTRAVENOUS |
2 products