FdaApplication
NDA 211950
Identifiers
- fda_app_no: NDA211950
Properties
| Property | Value |
|---|---|
| applicant_name | BAUSCH AND LOMB INC |
| application_type | NDA |
| approval_date | 2021-10-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| XIPERE | TRIAMCINOLONE ACETONIDE | 40MG/ML | SUSPENSION;INJECTION |
1 product