Generic Eliquis Sprinkle Availability
Last updated on Jun 11, 2025.
See also: Generic Eliquis
Eliquis Sprinkle is a brand name of apixaban, approved by the FDA in the following formulation(s):
ELIQUIS SPRINKLE (apixaban - for suspension;oral)
Is there a generic version of Eliquis Sprinkle available?
No. There is currently no therapeutically equivalent version of Eliquis Sprinkle available in the United States.
Note: Fraudulent online pharmacies may attempt to sell an illegal generic version of Eliquis Sprinkle. 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 FAQ.
Related patents
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.
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Apixaban formulations
Patent 11,896,586
Issued: February 13, 2024
Inventor(s): Badawy; Sherif Ibrahim Farag et al.
Assignee(s): Bristol-Myers Squibb Company (Princeton, NJ); Pfizer Inc. (New York, NY)Apixaban pharmaceutical formulation is provided. Also provided is a use of the apixaban formulation in treatment of a thromboembolic disorder.
Patent expiration dates:
- November 22, 2040✓✓
- November 22, 2040
-
Apixaban formulations
Patent 11896586*PE
Issued: February 13, 2024
Inventor(s): Badawy; Sherif Ibrahim Farag et al.
Assignee(s): Bristol-Myers Squibb Company (Princeton, NJ); Pfizer Inc. (New York, NY)Apixaban pharmaceutical formulation is provided. Also provided is a use of the apixaban formulation in treatment of a thromboembolic disorder.
Patent expiration dates:
- May 22, 2041
- May 22, 2041
-
Lactam-containing compounds and derivatives thereof as factor Xa inhibitors
Patent 6,967,208
Issued: November 22, 2005
Inventor(s): Pinto; Donald J. P. et al.
Assignee(s): Bristol-Myers Squibb Pharma Company (Princeton, NJ)The present application describes lactam-containing compounds and derivatives thereof of Formula I: ##STR1##
or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.Patent expiration dates:
- November 21, 2026✓✓✓
- November 21, 2026
-
Lactam-containing compounds and derivatives thereof as factor Xa inhibitors
Patent 6967208*PED
Issued: November 22, 2005
Inventor(s): Pinto; Donald J. P. et al.
Assignee(s): Bristol-Myers Squibb Pharma Company (Princeton, NJ)The present application describes lactam-containing compounds and derivatives thereof of Formula I: ##STR1##
or pharmaceutically acceptable salt forms thereof, wherein ring P, if present is a 5-7 membered carbocycle or heterocycle and ring M is a 5-7 membered carbocycle or heterocycle. Compounds of the present invention are useful as inhibitors of trypsin-like serine proteases, specifically factor Xa.Patent expiration dates:
- May 21, 2027✓
- May 21, 2027
Related exclusivities
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:
- April 17, 2028 - NEW PRODUCT
- October 17, 2028 - PEDIATRIC EXCLUSIVITY
More about Eliquis Sprinkle (apixaban)
- Check interactions
- Compare alternatives
- Imprints, shape & color data
- Side effects
- Dosage information
- During pregnancy
- Drug class: factor Xa inhibitors
- Breastfeeding
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Glossary
Term | Definition |
---|---|
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. |
Further information
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.