FdaApplication
ANDA 210436
Identifiers
- fda_app_no: ANDA210436
Properties
| Property | Value |
|---|---|
| applicant_name | SOLA PHARMACEUTICALS |
| application_type | ANDA |
| approval_date | 2021-03-26 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DIMETHYL FUMARATE | DIMETHYL FUMARATE | 240MG | CAPSULE, DELAYED RELEASE;ORAL |
| DIMETHYL FUMARATE | DIMETHYL FUMARATE | 120MG | CAPSULE, DELAYED RELEASE;ORAL |
2 products