FdaApplication
NDA 013621
Identifiers
- fda_app_no: NDA013621
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PERTOFRANE | DESIPRAMINE HYDROCHLORIDE | 50MG | CAPSULE;ORAL |
| PERTOFRANE | DESIPRAMINE HYDROCHLORIDE | 25MG | CAPSULE;ORAL |
2 products