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These highlights do not include all the information needed to use OXYMORPHONE HYDROCHLORIDE EXTENDED-RELEASE TABLETS safely and effectively. See full prescribing information for OXYMORPHONE HYDROCHLORIDE EXTENDED-RELEASE TABLETS. OXYMORPHONE HYDROCHLORIDE extended-release tablets, for oral use, CIIInitial U.S. Approval: 1959
Medication labelWhy this: Advisory · dailymed-prescription
Oxymorphone Hydrochloride Extended-Release Tablets are indicated for the management of severe and persistent pain that requires an opioid analgesic and that cannot be adequately treated with alternative options, including immediate-release opioids. Limitations of Usage Because of the risks of addiction, abuse, misuse, overdose and death, which can occur at any dosage or duration and persist over the course of therapy [see Warnings and Precautions (5.1)], reserve opioid analgesics, including Oxymorphone Hydrochloride Extended-Release Tablets, for use in patients for whom alternative treatment options are ineffective, not tolerated, or would be otherwise inadequate to provide sufficient management of pain. Oxymorphone Hydrochloride Extended-Release Tablets are not indicated as an as-needed (prn) analgesic.
- generic_name
- oxymorphone hydrochloride
- product_names
- Oxymorphone hydrochloride
- ndc
- 64896-695, 64896-696, 64896-697, 64896-698, 64896-699, 64896-700, 64896-701, 64896-695-08, 64896-695-13, 64896-695-01, 64896-695-03, 64896-696-08, 64896-696-13, 64896-696-01, 64896-696-03, 64896-697-08, 64896-697-13, 64896-697-01, 64896-697-03, 64896-698-01, 64896-698-03, 64896-698-08, 64896-698-13, 64896-699-08, 64896-699-13, 64896-699-01, 64896-699-03, 64896-700-08, 64896-700-13, 64896-700-01, 64896-700-03, 64896-701-08, 64896-701-13, 64896-701-01, 64896-701-03
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en