FDA Orange Book

Generic for Votrient

Votrient contains pazopanib. 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 Votrient is pazopanib. 6 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

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Votrient products in the Orange Book

Votrient products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
tablet, oralEQ 200MG BASEMarketed (Rx)AB5AB
tablet, oralEQ 400MG BASEDiscontinuedNone1None

NDA 022465, held by NOVARTIS PHARMACEUTICALS CORP. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic pazopanib

Approved generic versions of Votrient
CompanyANDATE codeApprovedStrengths
APOTEX INC217713AB (A-rated, therapeutically equivalent)October 19, 2023EQ 200MG BASE
SUN PHARMACEUTICAL INDUSTRIES LTD215837AB (A-rated, therapeutically equivalent)October 19, 2023EQ 200MG BASE
TEVA PHARMACEUTICALS INC217517AB (A-rated, therapeutically equivalent)October 19, 2023EQ 200MG BASE
NOVUGEN ONCOLOGY SDN BHD218231AB (A-rated, therapeutically equivalent)April 23, 2024EQ 200MG BASE
EUGIA PHARMA SPECIALITIES LTD219034AB (A-rated, therapeutically equivalent)December 4, 2024EQ 200MG BASE
TORRENT PHARMACEUTICALS LTD219922None (No TE code listed)September 4, 2025EQ 400MG BASE

Votrient NDC codes

Questions

Is there a generic for Votrient?

Yes. The generic name for Votrient is pazopanib. 6 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 Votrient?

The active ingredient in Votrient is pazopanib, 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.

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