FDA Orange Book
Is there a generic for Alvaiz?
Alvaiz contains eltrombopag choline. 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 Alvaiz (eltrombopag choline). The Orange Book shows its last listed patent expires November 5, 2038.
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Alvaiz products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| tablet, oral | EQ 18MG BASE | Marketed (Rx) | None | 0 | None |
| tablet, oral | EQ 36MG BASE | Marketed (Rx) | None | 0 | None |
| tablet, oral | EQ 54MG BASE | Marketed (Rx) | None | 0 | None |
| tablet, oral | EQ 9MG BASE | Marketed (Rx) | None | 0 | None |
NDA 216774, held by TEVA PHARMACEUTICALS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.
Alvaiz patents
| Patent | Expires | Covers | Use code | NDA |
|---|---|---|---|---|
| 11072586 | November 5, 2038 | Drug substance, Drug product | U-3936 | 216774 |
| 11072586 | November 5, 2038 | Drug substance, Drug product | U-3937 | 216774 |
| 11072586 | November 5, 2038 | Drug substance, Drug product | U-3938 | 216774 |
Alvaiz NDC codes
Questions
Is there a generic for Alvaiz?
No. The Orange Book lists no active FDA-approved generic (ANDA) for Alvaiz (eltrombopag choline). The Orange Book shows its last listed patent expires November 5, 2038.
What is the generic name for Alvaiz?
The active ingredient in Alvaiz is eltrombopag choline, per the FDA Orange Book.
When does the Alvaiz patent expire?
The last patent listed for Alvaiz in the Orange Book expires November 5, 2038. 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.