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Purple Book product · Reference 351(a)

Lartruvo

olaratumab

351(a)BLA 761038DiscVoluntarily Revoked Eli Lilly and Company

Oct 19, 2016

Approved

Reference 351(a)

License type

Disc

Marketing

None

Listed patents

Lartruvo (olaratumab) is Eli Lilly and Company's FDA-licensed reference biologic, approved under a 351(a) BLA in 2016. No biosimilars referencing Lartruvo are listed in the Purple Book yet.

Sourced from the FDA Purple Book · verified Jul 02, 2026

Key dates

  1. Approval

    Approval date of this BLA submission.

    Oct 19, 2016

    9 yr 11 mo ago

  2. Orphan exclusivity ends

    7-year orphan-drug exclusivity window.

    Feb 25, 2020

    6 yr 6 mo ago

  3. Today

Pharmaceutical detail

Strength

500MG/50ML (10MG/ML)

Dosage form

Injection

Route

Intravenous

Presentation

Single-Dose Vial

Center

CDER

License number

1891

Product number

001

Submission type

Original

Supplement number

Not listed

Change type

Not listed

Reference product family

View full family

This is the reference (originator) product. No biosimilars or interchangeables reference it in the Purple Book yet.

1 additional BLA record for this product (other strengths or presentations) are in the same reference family.

Patent list

No patent-list records were published for this product. The Purple Book patent list reflects the statutory patent exchange under the BPCIA and is not exhaustive.

Source provenance

Source kind · Advanced Search
Checked Jul 02, 2026
  • advanced-searchAdvanced Search · Jul 02, 2026
  • monthly-downloadMonthly download · Jul 02, 2026

Change history

  • v4Jul 02, 2026
  • v3Jul 02, 2026
  • v2Jul 02, 2026

Frequently asked questions

Does Lartruvo have approved biosimilars?

No 351(k) biosimilars or interchangeable biosimilars referencing Lartruvo are listed in the FDA Purple Book yet.

What is Lartruvo's BLA number?

Lartruvo is licensed under BLA 761038, held by Eli Lilly and Company.

When was Lartruvo approved by the FDA?

Lartruvo was approved by the FDA on Oct 19, 2016.

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