FdaApplication
ANDA 065113
Identifiers
- fda_app_no: ANDA065113
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2002-11-29 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMOXICILLIN | AMOXICILLIN | 400MG/5ML | FOR SUSPENSION;ORAL |
| AMOXICILLIN | AMOXICILLIN | 200MG/5ML | FOR SUSPENSION;ORAL |
2 products