Assyro AI

Purple Book product · Reference 351(a)

Riastap

Fibrinogen Concentrate (Human)

351(a)BLA 125317RxLicensed CSL Behring GmbH

Jan 16, 2009

Approved

Reference 351(a)

License type

Rx

Marketing

None

Listed patents

Riastap (Fibrinogen Concentrate (Human)) is CSL Behring GmbH's FDA-licensed reference biologic, approved under a 351(a) BLA in 2009. No biosimilars referencing Riastap 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.

    Jan 16, 2009

    17 yr 9 mo ago

  2. Orphan exclusivity ends

    7-year orphan-drug exclusivity window.

    Jan 16, 2016

    10 yr 8 mo ago

  3. Today

Pharmaceutical detail

Strength

900-1300MG

Dosage form

For Injection

Route

Intravenous

Presentation

Single-Dose Vial

Center

CBER

License number

1765

Product number

001

Submission type

Original

Supplement number

0

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
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Change history

  • v5Jul 02, 2026
  • v4Jul 02, 2026
  • v3Jul 02, 2026
  • v2Jul 02, 2026

Frequently asked questions

Does Riastap have approved biosimilars?

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

What is Riastap's BLA number?

Riastap is licensed under BLA 125317, held by CSL Behring GmbH.

When was Riastap approved by the FDA?

Riastap was approved by the FDA on Jan 16, 2009.

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