FdaApplication
ANDA 206939
Identifiers
- fda_app_no: ANDA206939
Properties
| Property | Value |
|---|---|
| applicant_name | AJENAT PHARMACEUTICALS LLC |
| application_type | ANDA |
| approval_date | 2017-02-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEFIXIME | CEFIXIME | 500MG/5ML | FOR SUSPENSION;ORAL |
1 product