FDA Orange Book

Is there a generic for Vonjo?

Vonjo contains pacritinib. 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 Vonjo (pacritinib). The Orange Book shows its last listed patent expires March 25, 2030 and its last listed exclusivity ends February 28, 2029.

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Vonjo products in the Orange Book

Vonjo products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
capsule, oralEQ 100MG BASEMarketed (Rx)None0None

NDA 208712, held by SOBI INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Vonjo patents

Patents listed for Vonjo
PatentExpiresCoversUse codeNDA
9573964May 5, 2028Method of useU-3332208712
9573964May 5, 2028Method of useU-3331208712
8153632January 17, 2029Drug substance, Drug productU-3332208712
8153632January 17, 2029Drug substance, Drug productU-3331208712
8980873March 25, 2030Drug substance, Drug productU-3331208712
8980873March 25, 2030Drug substance, Drug productU-3332208712

Vonjo exclusivity

Exclusivity listed for Vonjo
CodeMeaningExpiresNDA
NCENew chemical entityFebruary 28, 2027208712
ODE-397Orphan drug exclusivityFebruary 28, 2029208712

Vonjo NDC codes

Questions

Is there a generic for Vonjo?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Vonjo (pacritinib). The Orange Book shows its last listed patent expires March 25, 2030 and its last listed exclusivity ends February 28, 2029.

What is the generic name for Vonjo?

The active ingredient in Vonjo is pacritinib, per the FDA Orange Book.

When does the Vonjo patent expire?

The last patent listed for Vonjo in the Orange Book expires March 25, 2030. 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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