FDA Orange Book

Generic for Maxalt

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

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Maxalt products in the Orange Book

Maxalt products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
tablet, oralEQ 10MG BASEMarketed (Rx)AB6AB
tablet, oralEQ 5MG BASEDiscontinuedNone6AB

NDA 020864, held by ORGANON LLC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic rizatriptan benzoate

Approved generic versions of Maxalt
CompanyANDATE codeApprovedStrengths
AUROBINDO PHARMA LTD202490AB (A-rated, therapeutically equivalent)December 31, 2012EQ 10MG BASE, EQ 5MG BASE
PHARMAZONE202047AB (A-rated, therapeutically equivalent)December 31, 2012EQ 10MG BASE, EQ 5MG BASE
TEVA PHARMACEUTICALS USA077263AB (A-rated, therapeutically equivalent)December 31, 2012EQ 10MG BASE, EQ 5MG BASE
CHARTWELL RX SCIENCES LLC077526AB (A-rated, therapeutically equivalent)March 26, 2013EQ 10MG BASE, EQ 5MG BASE
MACLEODS PHARMACEUTICALS LTD203147AB (A-rated, therapeutically equivalent)February 11, 2014EQ 10MG BASE, EQ 5MG BASE
ALKEM LABORATORIES LTD203269AB (A-rated, therapeutically equivalent)February 18, 2016EQ 10MG BASE, EQ 5MG BASE

Maxalt NDC codes

Questions

Is there a generic for Maxalt?

Yes. The generic name for Maxalt is rizatriptan benzoate. 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 Maxalt?

The active ingredient in Maxalt is rizatriptan benzoate, 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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