FdaApplication
ANDA 206808
Identifiers
- fda_app_no: ANDA206808
Properties
| Property | Value |
|---|---|
| applicant_name | MACLEODS PHARMACEUTICALS LTD |
| application_type | ANDA |
| approval_date | 2024-09-20 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| CEVIMELINE HYDROCHLORIDE | CEVIMELINE HYDROCHLORIDE | 30MG | CAPSULE;ORAL |
1 product