FdaApplication
NDA 018841
Identifiers
- fda_app_no: NDA018841
Properties
| Property | Value |
|---|---|
| applicant_name | PFIZER INC |
| application_type | NDA |
| approval_date | 1992-10-29 |
Products (1)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| DAYPRO | OXAPROZIN | 600MG | TABLET;ORAL |
1 product