FdaApplication
NDA 018972
Identifiers
- fda_app_no: NDA018972
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 1985-12-24 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CORDARONE | AMIODARONE HYDROCHLORIDE | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
1 product