FdaApplication
ANDA 212769
Identifiers
- fda_app_no: ANDA212769
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMS |
| application_type | ANDA |
| approval_date | 2024-07-23 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SUCRALFATE | SUCRALFATE | 1GM/10ML | SUSPENSION;ORAL |
1 product