FdaApplication
NDA 020607
Identifiers
- fda_app_no: NDA020607
Properties
| Property | Value |
|---|---|
| applicant_name | PFIZER INC |
| application_type | NDA |
| approval_date | 1997-12-24 |
Products (2)
| Product | Active ingredient | Strength | Dosage form |
|---|---|---|---|
| ARTHROTEC | DICLOFENAC SODIUM; MISOPROSTOL | 50MG;0.2MG | TABLET, DELAYED RELEASE;ORAL |
| ARTHROTEC | DICLOFENAC SODIUM; MISOPROSTOL | 75MG;0.2MG | TABLET, DELAYED RELEASE;ORAL |
2 products