FdaApplication
ANDA 216232
Identifiers
- fda_app_no: ANDA216232
Properties
| Property | Value |
|---|---|
| applicant_name | MICRO LABS LTD |
| application_type | ANDA |
| approval_date | 2022-03-29 |
Products (3)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUOXETINE HYDROCHLORIDE | FLUOXETINE HYDROCHLORIDE | EQ 40MG BASE | CAPSULE;ORAL |
| FLUOXETINE HYDROCHLORIDE | FLUOXETINE HYDROCHLORIDE | EQ 20MG BASE | CAPSULE;ORAL |
| FLUOXETINE HYDROCHLORIDE | FLUOXETINE HYDROCHLORIDE | EQ 10MG BASE | CAPSULE;ORAL |
3 products