FdaApplication
NDA 018063
Identifiers
- fda_app_no: NDA018063
Properties
| Property | Value |
|---|---|
| applicant_name | USWM LLC |
| application_type | NDA |
| approval_date | 1986-10-28 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CORGARD | NADOLOL | 160MG | TABLET;ORAL |
| CORGARD | NADOLOL | 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| CORGARD | NADOLOL | 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| CORGARD | NADOLOL | 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| CORGARD | NADOLOL | 120MG | TABLET;ORAL |
5 products