FDA Orange Book

Generic for Ella

Ella contains ulipristal acetate. 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 Ella is ulipristal acetate. 1 company holds an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

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Ella products in the Orange Book

Ella products and approved generics
Form and routeStrengthBrand statusBrand TEActive genericsGeneric TE codes
tablet, oral30MGMarketed (Rx)AB1AB

NDA 022474, held by LABORATOIRE HRA PHARMA. Active generics are ANDA products in the Orange Book prescription list with the same ingredient, dosage form, route and strength.

Approved generic ulipristal acetate

Approved generic versions of Ella
CompanyANDATE codeApprovedStrengths
TEVA PHARMACEUTICALS USA207952AB (A-rated, therapeutically equivalent)February 13, 201730MG

Ella patents

Patents listed for Ella
PatentExpiresCoversUse codeNDA
9844510December 8, 2028Drug productNone022474
8735380February 20, 2029Drug productNone022474
9283233April 13, 2030Method of useU-1821022474
10159681April 13, 2030Method of useU-2510022474
10772897April 13, 2030Method of useU-2958022474
8512745June 2, 2030Drug productNone022474
8426392June 12, 2030Method of useU-1389022474
8962603June 12, 2030Method of useU-1657022474

Ella NDC codes

Questions

Is there a generic for Ella?

Yes. The generic name for Ella is ulipristal acetate. 1 company holds an active FDA approval (ANDA) for a generic version in the Orange Book. Therapeutic equivalence codes: AB.

What is the generic name for Ella?

The active ingredient in Ella is ulipristal acetate, per the FDA Orange Book.

When does the Ella patent expire?

The last patent listed for Ella in the Orange Book expires June 12, 2030. 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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