Generic RoxyBond Availability
ROXYBOND (oxycodone hydrochloride - tablet;oral)
Manufacturer: DAIICHI SANKYO INC
Approval date: April 20, 2017
Strength(s): 5MG, 15MG, 30MG
Has a generic version of RoxyBond been approved?
No. There is currently no therapeutically equivalent version of RoxyBond available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of RoxyBond. These medications may be counterfeit and potentially unsafe. If you purchase medications online, be sure you are buying from a reputable and valid online pharmacy. Ask your health care provider for advice if you are unsure about the online purchase of any medication.
See also: Generic Drug FAQs.
Patents are granted by the U.S. Patent and Trademark Office at any time during a drug's development and may include a wide range of claims.
Abuse resistant drugs, method of use and method of making
Issued: June 7, 2011
Inventor(s): Shah; Manish S. & Difalco; Ray J.
Assignee(s): Inspirion Delivery Technologies, LLC
An abuse resistant oral pharmaceutical composition, comprising: a barrier layer, comprising a first polymer; a diffusion layer, comprising a second polymer, substantially covering the barrier layer, wherein the diffusion layer is bonded to the barrier layer and comprises a drug that is substantially homogeneously distributed within the second polymer and diffuses from the diffusion layer within the gastrointestinal (GI) tract; and optionally an expansion layer comprising an expandable polymer, wherein the expansion layer is substantially covered by the barrier layer. Methods of making the same and methods of using the same are also provided.
Patent expiration dates:
- August 12, 2028✓
- August 12, 2028
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.
More about RoxyBond (oxycodone)
- RoxyBond Side Effects
- During Pregnancy or Breastfeeding
- Dosage Information
- Drug Images
- Drug Interactions
- Pricing & Coupons
- Drug class: narcotic analgesics
Related treatment guides
|Drug Patent||A drug patent is assigned by the U.S. Patent and Trademark Office and assigns exclusive legal right to the patent holder to protect the proprietary chemical formulation. The patent assigns exclusive legal right to the inventor or patent holder, and may include entities such as the drug brand name, trademark, product dosage form, ingredient formulation, or manufacturing process A patent usually expires 20 years from the date of filing, but can be variable based on many factors, including development of new formulations of the original chemical, and patent infringement litigation.|
|Drug Exclusivity||Exclusivity is the sole marketing rights granted by the FDA to a manufacturer upon the approval of a drug and may run simultaneously with a patent. Exclusivity periods can run from 180 days to seven years depending upon the circumstance of the exclusivity grant.|