FdaApplication
NDA 022020
Identifiers
- fda_app_no: NDA022020
Properties
| Property | Value |
|---|---|
| applicant_name | WYETH PHARMACEUTICALS LLC |
| application_type | NDA |
| approval_date | 2007-11-14 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| PROTONIX | PANTOPRAZOLE SODIUM | EQ 40MG BASE | FOR SUSPENSION, DELAYED RELEASE;ORAL |
1 product