FDA Orange Book

Generic for Vivlodex

Vivlodex contains meloxicam. 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 Vivlodex is meloxicam. 2 companies hold an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

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Vivlodex products in the Orange Book

Vivlodex products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
capsule, oral10MGDiscontinuedNone2AB
capsule, oral5MGDiscontinuedNone2AB

NDA 207233, held by ICEUTICA OPERATIONS LLC. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic meloxicam

Approved generic versions of Vivlodex
CompanyANDATE codeApprovedStrengths
LUPIN LTD209487AB (A-rated, therapeutically equivalent)June 1, 202010MG, 5MG
NOVITIUM PHARMA LLC211398AB (A-rated, therapeutically equivalent)March 9, 202110MG, 5MG

Vivlodex patents

Patents listed for Vivlodex
PatentExpiresCoversUse codeNDA
9526734March 31, 2033Drug productNone207233
9808468March 31, 2035Method of useU-2165207233
9808468March 31, 2035Method of useU-2160207233
9649318March 31, 2035Drug productNone207233

Questions

Is there a generic for Vivlodex?

Yes. The generic name for Vivlodex is meloxicam. 2 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 Vivlodex?

The active ingredient in Vivlodex is meloxicam, per the FDA Orange Book.

When does the Vivlodex patent expire?

The last patent listed for Vivlodex in the Orange Book expires March 31, 2035. 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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