FDA Orange Book
Generic for Viibryd
Viibryd contains vilazodone. 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 Viibryd is vilazodone. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
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Viibryd products in the Orange Book
| Form and route | Strength | Brand status | Brand TE | Active generics | Generic TE codes |
|---|---|---|---|---|---|
| tablet, oral | 10MG | Marketed (Rx) | AB | 5 | AB |
| tablet, oral | 20MG | Marketed (Rx) | AB | 5 | AB |
| tablet, oral | 40MG | Marketed (Rx) | AB | 5 | AB |
NDA 022567, 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 vilazodone
| Company | ANDA | TE code | Approved | Strengths |
|---|---|---|---|---|
| TEVA PHARMACEUTICALS USA | 208212 | AB (A-rated, therapeutically equivalent) | September 30, 2019 | 10MG, 20MG, 40MG |
| ALEMBIC PHARMACEUTICALS LTD | 208202 | AB (A-rated, therapeutically equivalent) | January 10, 2020 | 10MG, 20MG, 40MG |
| INVAGEN PHARMACEUTICALS INC | 208200 | AB (A-rated, therapeutically equivalent) | April 7, 2021 | 10MG, 20MG, 40MG |
| ACCORD HEALTHCARE INC | 208209 | AB (A-rated, therapeutically equivalent) | April 27, 2021 | 10MG, 20MG, 40MG |
| APOTEX INC | 208228 | AB (A-rated, therapeutically equivalent) | July 7, 2023 | 10MG, 20MG, 40MG |
Viibryd NDC codes
Questions
Is there a generic for Viibryd?
Yes. The generic name for Viibryd is vilazodone. 5 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.
What is the generic name for Viibryd?
The active ingredient in Viibryd is vilazodone, per the FDA Orange Book.
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.