FdaApplication
NDA 020988
Identifiers
- fda_app_no: NDA020988
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 2001-03-22 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROTONIX IV | PANTOPRAZOLE SODIUM | EQ 40MG BASE/VIAL | INJECTABLE;INTRAVENOUS |
1 product