FDA Orange Book

Is there a generic for Invega Trinza?

Invega Trinza contains paliperidone palmitate. 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 Invega Trinza (paliperidone palmitate). The Orange Book shows its last listed patent expires April 5, 2036.

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Invega Trinza products in the Orange Book

Invega Trinza products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
suspension, extended release, intramuscular273MG/0.875ML (273MG/0.875ML)Marketed (Rx)None0None
suspension, extended release, intramuscular410MG/1.315ML (311.79MG/ML)Marketed (Rx)None0None
suspension, extended release, intramuscular546MG/1.75ML (312MG/ML)Marketed (Rx)None0None
suspension, extended release, intramuscular819MG/2.625ML (312MG/ML)Marketed (Rx)None0None

NDA 207946, held by JANSSEN PHARMACEUTICALS INC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Invega Trinza patents

Patents listed for Invega Trinza
PatentExpiresCoversUse codeNDA
10143693April 5, 2036Method of useU-2458207946
10143693April 5, 2036Method of useU-2457207946

Invega Trinza NDC codes

Questions

Is there a generic for Invega Trinza?

No. The Orange Book lists no active FDA-approved generic (ANDA) for Invega Trinza (paliperidone palmitate). The Orange Book shows its last listed patent expires April 5, 2036.

What is the generic name for Invega Trinza?

The active ingredient in Invega Trinza is paliperidone palmitate, per the FDA Orange Book.

When does the Invega Trinza patent expire?

The last patent listed for Invega Trinza in the Orange Book expires April 5, 2036. 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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