FdaApplication
NDA 017535
Identifiers
- fda_app_no: NDA017535
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
| approval_date | 1988-07-06 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| LORELCO | PROBUCOL | 500MG | TABLET;ORAL |
| LORELCO | PROBUCOL | 250MG | TABLET;ORAL |
2 products