FdaApplication
NDA 017669
Identifiers
- fda_app_no: NDA017669
Properties
| Property | Value |
|---|---|
| applicant_name | SANOFI AVENTIS US LLC |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TENUATE | DIETHYLPROPION HYDROCHLORIDE | 75MG | TABLET, EXTENDED RELEASE;ORAL |
1 product