FdaApplication
NDA 018869
Identifiers
- fda_app_no: NDA018869
Properties
| Property | Value |
|---|---|
| applicant_name | BAYER PHARMACEUTICALS CORP |
| application_type | NDA |
| approval_date | 1988-12-28 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NIMOTOP | NIMODIPINE | 30MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE;ORAL |
1 product