FdaApplication
ANDA 211721
Identifiers
- fda_app_no: ANDA211721
Properties
| Property | Value |
|---|---|
| applicant_name | DR REDDYS LABORATORIES LTD |
| application_type | ANDA |
| approval_date | 2019-01-25 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUOXETINE HYDROCHLORIDE | FLUOXETINE HYDROCHLORIDE | EQ 60MG BASE | TABLET;ORAL |
1 product