Generic Triumeq Availability
TRIUMEQ (abacavir sulfate; dolutegravir sodium; lamivudine - tablet;oral)
Manufacturer: VIIV HLTHCARE
Approval date: August 22, 2014
Strength(s): EQ 600MG BASE;EQ 50MG BASE;300MG [RLD]
Has a generic version of Triumeq been approved?
No. There is currently no therapeutically equivalent version of Triumeq available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Triumeq. 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.
Carbocyclic nucleoside hemisulfate and its use in treating viral infections
Issued: September 25, 2001
Inventor(s): Brodie; Alastair Couper & Jones; Martin Francis & Seager; John Frederick & Wallis; Christopher John
Assignee(s): Glaxo Wellcome Inc.
The hemisulfate salt of (1S,4R)-cis-4-[2-amino-6-(cyclopropylamino)-9H-purin-9-yl]-2-cyclopentene- 1-methanol or a solvate of it is used in the treatment of viral infections.Patent expiration dates:
- May 14, 2018✓✓✓
- November 14, 2018✓
- May 14, 2018
Substituted 5-hydroxy-3,4,6,9,9a, 10-hexanhydro-2h-1-oxa04a,8a-diaza-anthracene-6,10-dioness
Issued: March 6, 2012
Inventor(s): Johns; Brian Alvin & Kawasuji; Takashi & Taishi; Teruhiko & Taoda; Yoshiyuki
Assignee(s): Shionogi & Co., Ltd. GlaxoSmithKline LLC
The present invention is directed to a class of substituted 5-hydroxy-3,4,6,9,9a,10-hexahydro-2H-1-oxa-4a,8a-diaza-anthracene-6,10-diones useful as anti-HIV agents. The compounds have the formula: Z═O; R20, R21, R22, R23, R24 and R25 independently are hydrogen, C1-C8 alkyl, (C6-C14)aryl-(C1-C8)alkyl, C6-C14 aryl, or alkoxy; the stereochemistry of an asymmetric carbon represented by * shows R- or S-configuration, or a mixture thereof; RX is hydrogen; R14 is hydrogen or optionally substituted lower alkyl; R3 is hydrogen; R1 is hydrogen or lower alkyl; R is halogen; and m is 1, 2 or 3; or a pharmaceutically acceptable salt thereof.Patent expiration dates:
- October 5, 2027✓✓
- October 5, 2027
Synthesis of carbamoylpyridone HIV integrase inhibitors and intermediates
Issued: January 26, 2016
Assignee(s): SHIONOGI & CO., LTD. ViiV Healthcare Company
A synthesis approach providing an early ring attachment via a bromination to compound 1-1 yielding compound II-II, whereby a final product such as AA can be synthesized. In particular, the 2,4-difluorophenyl-containing sidechain is attached before creation of the additional ring Q.Patent expiration dates:
- December 8, 2029✓✓
- December 8, 2029
Exclusivity is exclusive marketing rights granted by the FDA upon approval of a drug and can run concurrently with a patent or not. Exclusivity is a statutory provision and is granted to an NDA applicant if statutory requirements are met.
- Exclusivity expiration dates:
- August 12, 2018 - NEW CHEMICAL ENTITY
More about Triumeq (abacavir / dolutegravir / lamivudine)
- Triumeq Side Effects
- During Pregnancy
- Dosage Information
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- Drug class: antiviral combinations
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.|
|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.|