FdaApplication
NDA 021746
Identifiers
- fda_app_no: NDA021746
Properties
| Property | Value |
|---|---|
| applicant_name | LEES PHARMACEUTICAL HK LTD |
| application_type | NDA |
| approval_date | 2012-03-06 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SURFAXIN | LUCINACTANT | 8.5ML | SUSPENSION;INTRATRACHEAL |
1 product