FDA Orange Book

Is there a generic for Yuvezzi?

Yuvezzi contains carbachol and brimonidine. 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 Yuvezzi (carbachol and brimonidine). The Orange Book shows its last listed patent expires November 10, 2042 and its last listed exclusivity ends January 28, 2029.

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Yuvezzi products in the Orange Book

Yuvezzi products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
solution/drops, ophthalmic0.1%;2.75%Marketed (Rx)None0None

NDA 220142, held by VISUS THERAPEUTICS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Yuvezzi patents

Patents listed for Yuvezzi
PatentExpiresCoversUse codeNDA
8455494May 24, 2030Method of useU-3741220142
8455494May 24, 2030Method of useU-4419220142
8455494May 24, 2030Method of useU-4420220142
12268662November 10, 2042Drug productU-3741220142
12268662November 10, 2042Drug productU-4419220142
12268662November 10, 2042Drug productU-4420220142

Yuvezzi exclusivity

Exclusivity listed for Yuvezzi
CodeMeaningExpiresNDA
NPNew productJanuary 28, 2029220142

Yuvezzi NDC codes

Questions

Is there a generic for Yuvezzi?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Yuvezzi (carbachol and brimonidine). The Orange Book shows its last listed patent expires November 10, 2042 and its last listed exclusivity ends January 28, 2029.

What is the generic name for Yuvezzi?

The active ingredient in Yuvezzi is carbachol and brimonidine, per the FDA Orange Book.

When does the Yuvezzi patent expire?

The last patent listed for Yuvezzi in the Orange Book expires November 10, 2042. 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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