FdaApplication
ANDA 078861
Identifiers
- fda_app_no: ANDA078861
Properties
| Property | Value |
|---|---|
| applicant_name | AUROBINDO PHARMA LTD |
| application_type | ANDA |
| approval_date | 2008-10-31 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SERTRALINE HYDROCHLORIDE | SERTRALINE HYDROCHLORIDE | EQ 20MG BASE/ML | CONCENTRATE;ORAL |
1 product