FdaApplication
ANDA 212492
Identifiers
- fda_app_no: ANDA212492
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2019-11-26 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| AMINOCAPROIC ACID | AMINOCAPROIC ACID | 500MG | TABLET;ORAL |
1 product