FdaApplication
NDA 209463
Identifiers
- fda_app_no: NDA209463
Properties
| Property | Value |
|---|---|
| applicant_name | HIKMA PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 2017-06-30 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PANTOPRAZOLE SODIUM | PANTOPRAZOLE SODIUM | EQ 40MG BASE/VIAL | POWDER;INTRAVENOUS |
1 product