FdaApplication
NDA 011722
Identifiers
- fda_app_no: NDA011722
Properties
| Property | Value |
|---|---|
| applicant_name | MPP PHARMA LLC |
| application_type | NDA |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| TENUATE | DIETHYLPROPION HYDROCHLORIDE | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product