FdaApplication
NDA 019002
Identifiers
- fda_app_no: NDA019002
Properties
| Property | Value |
|---|---|
| applicant_name | JOHNSON AND JOHNSON PHARMACEUTICAL RESEARCH AND DEVELOPMENT LLC |
| application_type | NDA |
| approval_date | 1990-12-28 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VASCOR | BEPRIDIL HYDROCHLORIDE | 400MG | TABLET;ORAL |
| VASCOR | BEPRIDIL HYDROCHLORIDE | 300MG | TABLET;ORAL |
| VASCOR | BEPRIDIL HYDROCHLORIDE | 200MG | TABLET;ORAL |
3 products