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Purple Book product · Reference 351(a)

Sylvant

siltuximab

351(a)BLA 125496RxLicensed Recordati Rare Diseases, Inc.

Apr 23, 2014

Approved

Reference 351(a)

License type

Rx

Marketing

None

Listed patents

Sylvant (siltuximab) is Recordati Rare Diseases, Inc.'s FDA-licensed reference biologic, approved under a 351(a) BLA in 2014. No biosimilars referencing Sylvant 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.

    Apr 23, 2014

    12 yr 5 mo ago

  2. Orphan exclusivity ends

    7-year orphan-drug exclusivity window.

    Apr 23, 2021

    5 yr 4 mo ago

  3. Today

Pharmaceutical detail

Strength

400MG

Dosage form

For Injection

Route

Intravenous

Presentation

Single-Dose Vial

Center

CDER

License number

1899

Product number

002

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 Sylvant have approved biosimilars?

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

What is Sylvant's BLA number?

Sylvant is licensed under BLA 125496, held by Recordati Rare Diseases, Inc..

When was Sylvant approved by the FDA?

Sylvant was approved by the FDA on Apr 23, 2014.

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