FdaApplication
NDA 019915
Identifiers
- fda_app_no: NDA019915
Properties
| Property | Value |
|---|---|
| applicant_name | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE |
| application_type | NDA |
| approval_date | 1991-05-16 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| MONOPRIL | FOSINOPRIL SODIUM | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| MONOPRIL | FOSINOPRIL SODIUM | 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| MONOPRIL | FOSINOPRIL SODIUM | 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
3 products