FdaApplication
NDA 021235
Identifiers
- fda_app_no: NDA021235
Properties
| Property | Value |
|---|---|
| applicant_name | ELI LILLY AND CO |
| application_type | NDA |
| approval_date | 2001-02-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROZAC WEEKLY | FLUOXETINE HYDROCHLORIDE | EQ 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** | CAPSULE, DELAYED REL PELLETS;ORAL |
1 product