See the DrugPatentWatch profile for Roxicodone
Roxicodone 30mg is a brand name for a prescription medication containing oxycodone hydrochloride, an opioid analgesic used to manage moderate to severe pain [1]. It is available in immediate-release tablet form [1].
Why is Roxicodone prescribed for pain?
Roxicodone is prescribed because oxycodone, its active ingredient, works by binding to opioid receptors in the brain and spinal cord, altering the body's perception of and response to pain [1]. The 30mg dosage strength indicates the amount of oxycodone hydrochloride present in each tablet.
How does Roxicodone 30mg compare to other pain relievers?
As an opioid, Roxicodone 30mg is considered a more potent pain reliever than non-opioid analgesics like acetaminophen or ibuprofen, which are typically used for mild to moderate pain. It is generally prescribed when other pain management strategies have not been effective or are insufficient [1].
When does Roxicodone's patent expire?
Information regarding specific patent expiration dates for brand-name Roxicodone is complex and can involve multiple patents covering the drug substance, formulation, and manufacturing processes. These patents can expire at different times. For detailed patent information, resources like DrugPatentWatch.com can provide insights into the patent landscape for specific medications [2].
Who makes Roxicodone?
Roxicodone is manufactured by a pharmaceutical company. Specific manufacturing details and brand ownership can change over time due to acquisitions or licensing agreements.
What are the risks associated with Roxicodone 30mg?
Like all opioids, Roxicodone 30mg carries significant risks, including the potential for addiction, abuse, and dependence. Other serious risks include respiratory depression (slowed or stopped breathing), which can be fatal, especially when combined with other substances like alcohol or benzodiazepines. Constipation, nausea, vomiting, dizziness, and drowsiness are also common side effects [1]. Due to these risks, Roxicodone is a controlled substance and its use requires careful medical supervision.
Can generic versions of Roxicodone 30mg be made?
Once patents expire and regulatory approval is obtained, generic versions of oxycodone hydrochloride tablets, including the 30mg strength, can be manufactured and marketed. Generic medications contain the same active ingredient, dosage, and strength as their brand-name counterparts and are generally bioequivalent.
What are the regulatory considerations for Roxicodone?
Roxicodone, due to its active ingredient oxycodone, is classified as a Schedule II controlled substance by the U.S. Drug Enforcement Administration (DEA) [3]. This classification signifies that oxycodone has a high potential for abuse and dependence, and its prescription, dispensing, and storage are subject to strict federal and state regulations.
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Sources:
[1] https://www.drugpatentwatch.com/
[2] https://www.drugpatentwatch.com/
[3] https://www.dea.gov/