FDA Orange Book
Generic for Vuity
Vuity contains pilocarpine. 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
Yes. The generic name for Vuity is pilocarpine. 1 company holds an active FDA approval (ANDA) for a generic version in the Orange Book.
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Vuity products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| solution/drops, ophthalmic | 1.25% | Discontinued | None | 1 | None |
NDA 214028, held by ABBVIE INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Approved generic pilocarpine
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| AMNEAL EU LTD | 217733 | None (No TE code listed) | April 28, 2025 | 1.25% |
Vuity patents
| Patent | Expires | Covers | Use code | NDA |
|---|---|---|---|---|
| 10610518 | April 24, 2039 | Method of use | U-3562 | 214028 |
| 10610518 | April 24, 2039 | Method of use | U-3561 | 214028 |
| 11285134 | April 24, 2039 | Method of use | U-3561 | 214028 |
| 11285134 | April 24, 2039 | Method of use | U-3562 | 214028 |
| 11285134 | April 24, 2039 | Method of use | U-3252 | 214028 |
| 10610518 | April 24, 2039 | Method of use | U-3252 | 214028 |
Vuity exclusivity
| Code | Meaning | Expires | NDA |
|---|---|---|---|
| D-187 | New dosing schedule | March 28, 2026 | 214028 |
Questions
Is there a generic for Vuity?
Yes. The generic name for Vuity is pilocarpine. 1 company holds an active FDA approval (ANDA) for a generic version in the Orange Book.
What is the generic name for Vuity?
The active ingredient in Vuity is pilocarpine, per the FDA Orange Book.
When does the Vuity patent expire?
The last patent listed for Vuity in the Orange Book expires April 24, 2039. 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.