# EMRELIS — FDA application BLA761384

Informational only - not investment advice.

Application BLA761384 · type BLA · FDA status: approved · original approval 2025-05-14

Listed sponsor: ABBVIE INC · [ABBV company profile](/company/ABBV/) · exact_unique

Sponsor as listed in Drugs@FDA at retrieval (2026-08-07); FDA sponsor listings can lag ownership transfers.

## FDA application facts

| Product | FDA-listed trade name | Active ingredient | Dosage form | Route | Strength | Marketing status | TE code | RLD |
| --- | --- | --- | --- | --- | --- | --- | --- | --- |
| 001 | EMRELIS | TELISOTUZUMAB VEDOTIN-TLLV | VIAL | SINGLE-DOSE | 20MG | Prescription | not listed | not listed |
| 002 | EMRELIS | TELISOTUZUMAB VEDOTIN-TLLV | VIAL | SINGLE-DOSE | 100MG | Prescription | not listed | not listed |

## Orange Book patent and exclusivity listings

Patent/exclusivity listings: not applicable — the FDA Orange Book covers NDA and ANDA small-molecule applications, not BLA biologics.

## Compound cross-links

- TELISOTUZUMAB VEDOTIN · UNII 976X9VXC3Z · no lmmol compound match

Ingredient–compound links use FDA openFDA/GSRS identifiers and an exact lmmol InChIKey join. Ingredient names cannot create a link.

## Related pages

- [Sponsor company](/company/ABBV/)
- [FDA-approved application index](/drug/)
- [Large-cap biopharma](/compare/pharma/)

Sources: https://www.fda.gov/drugs/drug-approvals-and-databases/drugsfda-data-files · https://www.fda.gov/drugs/drug-approvals-and-databases/orange-book-data-files · https://api.fda.gov/drug/drugsfda.json?search=application_number:BLA761384. FDA data retrieved 2026-08-07.

Regulatory listing data as published by FDA; not medical or investment advice.