FdaApplication
ANDA 209351
Identifiers
- fda_app_no: ANDA209351
Properties
| Property | Value |
|---|---|
| applicant_name | DEVA HOLDING AS |
| application_type | ANDA |
| approval_date | 2023-09-13 |
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