FdaApplication
ANDA 075787
Identifiers
- fda_app_no: ANDA075787
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | ANDA |
| approval_date | 2002-01-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUOXETINE | FLUOXETINE HYDROCHLORIDE | EQ 10MG BASE | CAPSULE;ORAL |
| FLUOXETINE | FLUOXETINE HYDROCHLORIDE | EQ 20MG BASE | CAPSULE;ORAL |
2 products