FdaApplication
NDA 021858
Identifiers
- fda_app_no: NDA021858
Properties
| Property | Value |
|---|---|
| applicant_name | HOFFMANN LA ROCHE INC |
| application_type | NDA |
| approval_date | 2006-01-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BONIVA | IBANDRONATE SODIUM | EQ 3MG BASE/3ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | INJECTABLE;INTRAVENOUS |
1 product