FdaApplication
ANDA 079121
Identifiers
- fda_app_no: ANDA079121
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMA CANADA INC |
| application_type | ANDA |
| approval_date | 2012-05-03 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ESCITALOPRAM OXALATE | ESCITALOPRAM OXALATE | EQ 5MG BASE/5ML | SOLUTION;ORAL |
1 product