FDA Orange Book

Generic for Selzentry

Selzentry contains maraviroc. 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 Selzentry is maraviroc. 4 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB. Generics match 2 of the 5 Selzentry products the Orange Book lists.

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Selzentry products in the Orange Book

Selzentry products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
solution, oral20MG/MLMarketed (Rx)None0None
tablet, oral150MGMarketed (Rx)AB4AB
tablet, oral25MGDiscontinuedNone0None
tablet, oral300MGMarketed (Rx)AB4AB
tablet, oral75MGDiscontinuedNone0None

NDA 208984, 022128, held by VIIV HEALTHCARE CO. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic maraviroc

Approved generic versions of Selzentry
CompanyANDATE codeApprovedStrengths
HETERO LABS LTD UNIT III203347AB (A-rated, therapeutically equivalent)February 7, 2022150MG, 300MG
PHARMAZONE217114AB (A-rated, therapeutically equivalent)August 17, 2023150MG, 300MG
NAVINTA LLC217880AB (A-rated, therapeutically equivalent)May 13, 2025150MG, 300MG
RHODES PHARMACEUTICALS LP216143AB (A-rated, therapeutically equivalent)November 4, 2025150MG, 300MG

Selzentry NDC codes

Questions

Is there a generic for Selzentry?

Yes. The generic name for Selzentry is maraviroc. 4 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB. Generics match 2 of the 5 Selzentry products the Orange Book lists.

What is the generic name for Selzentry?

The active ingredient in Selzentry is maraviroc, 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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