FdaApplication
NDA 020154
Identifiers
- fda_app_no: NDA020154
Properties
| Property | Value |
|---|---|
| applicant_name | BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE |
| application_type | NDA |
| approval_date | 1991-10-09 |
Products (5)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| VIDEX | DIDANOSINE | 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
| VIDEX | DIDANOSINE | 200MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
| VIDEX | DIDANOSINE | 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
| VIDEX | DIDANOSINE | 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
| VIDEX | DIDANOSINE | 150MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | TABLET, CHEWABLE;ORAL |
5 products