approval · primary record
OXAPROZIN POTASSIUM
FDA · NDA · 2024-11-21
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2024-11-21 |
| Brand | DAYPRO ALTA |
| Sponsor | PFIZER |
| Route | ORAL |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:35:11.939Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:OXAPROZIN POTASSIUM:2024-11-21
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