FdaApplication
ANDA 065207
Identifiers
- fda_app_no: ANDA065207
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES LTD |
| application_type | ANDA |
| approval_date | 2007-01-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMOXICILLIN AND CLAVULANATE POTASSIUM | AMOXICILLIN; CLAVULANATE POTASSIUM | 600MG/5ML;EQ 42.9MG BASE/5ML | FOR SUSPENSION;ORAL |
1 product