FdaApplication
ANDA 210962
Identifiers
- fda_app_no: ANDA210962
Properties
| Property | Value |
|---|---|
| applicant_name | AMNEAL EU LTD |
| application_type | ANDA |
| approval_date | 2024-07-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| BROMFENAC SODIUM | BROMFENAC SODIUM | EQ 0.07% ACID | SOLUTION/DROPS;OPHTHALMIC |
1 product