FdaApplication
ANDA 216606
Identifiers
- fda_app_no: ANDA216606
Properties
| Property | Value |
|---|---|
| applicant_name | AMTA LABS LTD |
| application_type | ANDA |
| approval_date | 2023-04-10 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| NISOLDIPINE | NISOLDIPINE | 8.5MG | TABLET, EXTENDED RELEASE;ORAL |
| NISOLDIPINE | NISOLDIPINE | 17MG | TABLET, EXTENDED RELEASE;ORAL |
2 products