FdaApplication
NDA 020707
Identifiers
- fda_app_no: NDA020707
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1997-03-07 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SKELID | TILUDRONATE DISODIUM | EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product