FdaApplication
NDA 215910
Identifiers
- fda_app_no: NDA215910
Properties
| Property | Value |
|---|---|
| applicant_name | SUN PHARMACEUTICAL INDUSTRIES INC |
| application_type | NDA |
| approval_date | 2022-11-17 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| SEZABY | PHENOBARBITAL SODIUM | 100MG/VIAL | POWDER;INTRAVENOUS |
1 product