FDA Orange Book

Is there a generic for Eliquis Sprinkle?

Eliquis Sprinkle contains apixaban. Orange Book status for every listed strength, the approved generic makers, and the listed patents and exclusivities.

Source: FDA Orange Book data file dated 2026-10-09. Publisher page

No. The Orange Book lists no active FDA-approved generic (ANDA) for Eliquis Sprinkle (apixaban). The Orange Book shows its last listed patent expires May 22, 2041 and its last listed exclusivity ends October 17, 2028.

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Eliquis Sprinkle products in the Orange Book

Eliquis Sprinkle products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
for suspension, oral0.15MGMarketed (Rx)None0None

NDA 220073, held by BRISTOL MYERS SQUIBB CO. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Eliquis Sprinkle patents

Patents listed for Eliquis Sprinkle
PatentExpiresCoversUse codeNDA
6967208November 21, 2026Drug substance, Drug productU-4180220073
6967208*PEDMay 21, 2027Method of useNone220073
11896586November 22, 2040Drug productU-4180220073
11896586*PEDMay 22, 2041Method of useNone220073

Eliquis Sprinkle exclusivity

Exclusivity listed for Eliquis Sprinkle
CodeMeaningExpiresNDA
NPNew productApril 17, 2028220073
PEDPediatric exclusivityOctober 17, 2028220073

Eliquis Sprinkle NDC codes

Questions

Is there a generic for Eliquis Sprinkle?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Eliquis Sprinkle (apixaban). The Orange Book shows its last listed patent expires May 22, 2041 and its last listed exclusivity ends October 17, 2028.

What is the generic name for Eliquis Sprinkle?

The active ingredient in Eliquis Sprinkle is apixaban, per the FDA Orange Book.

When does the Eliquis Sprinkle patent expire?

The last patent listed for Eliquis Sprinkle in the Orange Book expires May 22, 2041. A listed patent expiry date is not a generic launch date.

What does a therapeutic equivalence code mean?

In the Orange Book, codes that start with A (such as AB) mean FDA considers the product therapeutically equivalent to the reference drug. Codes that start with B mean FDA does not, at this time, consider the product therapeutically equivalent.

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