FDA Orange Book

Is there a generic for Vizz?

Vizz contains aceclidine. 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 Vizz (aceclidine). The Orange Book shows its last listed patent expires March 15, 2044 and its last listed exclusivity ends July 31, 2030.

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Vizz products in the Orange Book

Vizz products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
solution/drops, ophthalmicEQ 1.44% BASEMarketed (Rx)None0None

NDA 218585, held by LENZ THERAPEUTICS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Vizz patents

Patents listed for Vizz
PatentExpiresCoversUse codeNDA
10052313March 24, 2034Drug productU-3741218585
9844537March 24, 2034Drug productU-3741218585
11179328March 24, 2034Method of useU-3741218585
12653779June 18, 2035Method of useU-3741218585
12533347October 8, 2039Method of useU-3741218585
12128036October 8, 2039Method of useU-3741218585
12414942March 15, 2044Method of useU-3741218585

Vizz exclusivity

Exclusivity listed for Vizz
CodeMeaningExpiresNDA
NCENew chemical entityJuly 31, 2030218585

Vizz NDC codes

Questions

Is there a generic for Vizz?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Vizz (aceclidine). The Orange Book shows its last listed patent expires March 15, 2044 and its last listed exclusivity ends July 31, 2030.

What is the generic name for Vizz?

The active ingredient in Vizz is aceclidine, per the FDA Orange Book.

When does the Vizz patent expire?

The last patent listed for Vizz in the Orange Book expires March 15, 2044. 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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