Generic Metvixia Availability
METVIXIA (methyl aminolevulinate hydrochloride - cream; topical)
Has a generic version of Metvixia been approved?
No. There is currently no therapeutically equivalent version of Metvixia available.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Metvixia. 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: About generic drugs.
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.
Esters of 5-aminolevulinic acid as photosensitizing agents in photochemotherapy
Issued: March 7, 2000
Inventor(s): Gierskcky; Karl E. & Moan; Johan & Peng; Qian & Steen; Harald & Warloe; Trond & Bjorseth; Alf
Assignee(s): PhotoCure AS
The invention provides a pharmaceutical compositions comprising a compound of formula I: EQU R.sub.2.sup.2 N--CH.sub.2 COCH.sub.2 --CH.sub.2 CO--OR.sup.1(I) wherein, R.sup.1 and R.sup.2 have any of the values defined in the specification; or a salt thereof; and a pharmaceutically acceptable carrier or excipient. The invention also provides a method for the diagnosis or photochemotherapeutic treatment of disorders or abnormalities of external or internal surfaces of the body using such compounds or salts.Patent expiration dates:
- March 8, 2016✓
- March 8, 2016
- Metvixia Consumer Information (Drugs.com)
- Metvixia cream Consumer Information (Wolters Kluwer)
- Metvixia topical Consumer Information (Cerner Multum)
- Metvixia Advanced Consumer Information (Micromedex)
- Methyl aminolevulinate cream Consumer Information (Wolters Kluwer)
- Methyl aminolevulinate topical Consumer Information (Cerner Multum)
- Methyl aminolevulinate Topical application Advanced Consumer Information (Micromedex)
|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.|
|RLD||A Reference Listed Drug (RLD) is an approved drug product to which new generic versions are compared to show that they are bioequivalent. A drug company seeking approval to market a generic equivalent must refer to the Reference Listed Drug in its Abbreviated New Drug Application (ANDA). By designating a single reference listed drug as the standard to which all generic versions must be shown to be bioequivalent, FDA hopes to avoid possible significant variations among generic drugs and their brand name counterpart.|