FdaApplication
NDA 019815
Identifiers
- fda_app_no: NDA019815
Properties
| Property | Value |
|---|---|
| applicant_name | TAKEDA PHARMACEUTICALS USA INC |
| application_type | NDA |
| approval_date | 1996-09-06 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROAMATINE | MIDODRINE HYDROCHLORIDE | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| PROAMATINE | MIDODRINE HYDROCHLORIDE | 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| PROAMATINE | MIDODRINE HYDROCHLORIDE | 2.5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
3 products