FdaApplication
NDA 018647
Identifiers
- fda_app_no: NDA018647
Properties
| Property | Value |
|---|---|
| applicant_name | KING PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 1983-05-25 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CORZIDE | BENDROFLUMETHIAZIDE; NADOLOL | 5MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| CORZIDE | BENDROFLUMETHIAZIDE; NADOLOL | 5MG;80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
2 products