approval · primary record
OXYMORPHONE HYDROCHLORIDE
FDA · NDA · 2024-10-31
| Agency | FDA |
|---|---|
| Submission type | NDA |
| Action date | 2024-10-31 |
| Brand | OPANA ER |
| Sponsor | ENDO OPERATIONS |
| Route | ORAL |
Provenance
- Source: openFDA Drugs@FDA
- Fetched at: 2026-10-28T02:35:23.130Z
- Licence class: public-domain
- Verdict: primary-source
- Entity id: FDA:OXYMORPHONE HYDROCHLORIDE:2024-10-31
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