FdaApplication
ANDA 217655
Identifiers
- fda_app_no: ANDA217655
Properties
| Property | Value |
|---|---|
| applicant_name | SOMERSET THERAPEUTICS LLC |
| application_type | ANDA |
| approval_date | 2023-06-16 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| FAMOTIDINE | FAMOTIDINE | 40MG/5ML | FOR SUSPENSION;ORAL |
1 product