FdaApplication
ANDA 075690
Identifiers
- fda_app_no: ANDA075690
Properties
| Property | Value |
|---|---|
| applicant_name | ACTAVIS MID ATLANTIC LLC |
| application_type | ANDA |
| approval_date | 2002-01-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FLUOXETINE HYDROCHLORIDE | FLUOXETINE HYDROCHLORIDE | EQ 20MG BASE/5ML | SOLUTION;ORAL |
1 product