FdaApplication
NDA 019898
Identifiers
- fda_app_no: NDA019898
Properties
| Property | Value |
|---|---|
| applicant_name | BRISTOL MYERS SQUIBB |
| application_type | NDA |
| approval_date | 1991-10-31 |
Products (4)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PRAVACHOL | PRAVASTATIN SODIUM | 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| PRAVACHOL | PRAVASTATIN SODIUM | 80MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| PRAVACHOL | PRAVASTATIN SODIUM | 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
| PRAVACHOL | PRAVASTATIN SODIUM | 40MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET;ORAL |
4 products