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Purple Book product · Reference 351(a)

Eylea

aflibercept

351(a)BLA 125387RxLicensed Regeneron Pharmaceuticals, Inc.

Nov 18, 2011

Approved

Reference 351(a)

License type

Rx

Marketing

88

Listed patents

Eylea (aflibercept) is Regeneron Pharmaceuticals, Inc.'s FDA-licensed reference biologic, approved under a 351(a) BLA in 2011. The FDA Purple Book lists 88 published patents for it, the last expiring 2042. 6 approved follow-on biologics reference Eylea (Yesafili, Opuviz, Ahzantive, Enzeevu, Pavblu, and Eydenzelt). Its 12-year reference-product exclusivity under the BPCIA is listed as ending May 18, 2024.

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

Key dates

  1. First licensure

    Date the BLA was first licensed.

    Nov 18, 2011

    14 yr 11 mo ago

  2. Approval

    Approval date of this BLA submission.

    Nov 18, 2011

    14 yr 11 mo ago

  3. Reference product exclusivity ends

    12-year reference-product exclusivity window per BPCIA §351(k)(7).

    May 18, 2024

    2 yr 2 mo ago

  4. Today

  5. Orphan exclusivity ends

    7-year orphan-drug exclusivity window.

    Feb 08, 2030

    in 3 yr 7 mo

Pharmaceutical detail

Strength

2MG/0.05ML

Dosage form

Injection

Route

Intravitreal

Presentation

Single-Dose Vial

Center

CDER

License number

1760

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. Its approved biosimilars and interchangeables are listed below.

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

Patent list (88)

Patents published in the FDA Purple Book Patent List for this product, with expiration date and source link.
PatentExpiresInSource
10,857,231Mar 14, 20224 yr 5 mo agoFDA
7,070,959Jun 16, 20233 yr 2 mo agoFDA
10,406,226Mar 22, 20264 mo agoFDA
10,464,992Jun 14, 2027in 11 moFDA
11,066,458Jun 14, 2027in 11 moFDA
11,084,865Jun 14, 2027in 11 moFDA
11,732,024Jun 14, 2027in 11 moFDA
10,415,055Jun 04, 2028in 1 yr 11 moFDA
9,562,238Jun 04, 2028in 1 yr 11 moFDA
9,932,605Jun 04, 2028in 1 yr 11 moFDA
7,771,997Jul 02, 2028in 2 yrFDA
9,222,106Jul 02, 2028in 2 yrFDA
10,130,681Jan 11, 2032in 5 yr 7 moFDA
10,828,345Jan 11, 2032in 5 yr 7 moFDA
10,857,205Jan 11, 2032in 5 yr 7 moFDA
10,888,601Jan 11, 2032in 5 yr 7 moFDA
11,253,572Jan 11, 2032in 5 yr 7 moFDA
11,559,564Jan 11, 2032in 5 yr 7 moFDA
11,707,506Jan 11, 2032in 5 yr 7 moFDA
11,975,045Jan 11, 2032in 5 yr 7 moFDA
11,986,511Jan 11, 2032in 5 yr 7 moFDA
12,268,730Jan 11, 2032in 5 yr 7 moFDA
9,669,069Jan 11, 2032in 5 yr 7 moFDA
9,254,338May 22, 2032in 5 yr 11 moFDA
11,332,771Mar 14, 2034in 7 yr 9 moFDA
11,970,724Mar 14, 2034in 7 yr 9 moFDA
D858,754Sep 03, 2034in 8 yr 3 moFDA
9,315,281Sep 16, 2034in 8 yr 3 moFDA
11,268,109Oct 21, 2035in 9 yr 5 moFDA
11,788,102Oct 21, 2035in 9 yr 5 moFDA
9,816,110Oct 21, 2035in 9 yr 5 moFDA
D906,102Dec 29, 2035in 9 yr 7 moFDA
10,927,342Aug 03, 2036in 10 yr 2 moFDA
11,312,936Aug 03, 2036in 10 yr 2 moFDA
12,221,619Aug 03, 2036in 10 yr 2 moFDA
D934,069Oct 26, 2036in 10 yr 5 moFDA
11,549,154Dec 25, 2036in 10 yr 7 moFDA
10,669,594Feb 12, 2037in 10 yr 9 moFDA
11,918,785Jun 29, 2037in 11 yr 1 moFDA
10,182,969Jul 13, 2037in 11 yr 2 moFDA
D961,376Aug 23, 2037in 11 yr 3 moFDA
D961,377Aug 23, 2037in 11 yr 3 moFDA
11,577,025Oct 06, 2037in 11 yr 5 moFDA
11,680,930Oct 25, 2037in 11 yr 5 moFDA
10,905,786Mar 06, 2038in 11 yr 10 moFDA
10,918,754Mar 06, 2038in 11 yr 10 moFDA
12,116,622May 25, 2038in 12 yrFDA
11,769,597Aug 15, 2038in 12 yr 3 moFDA
11,433,186Dec 12, 2038in 12 yr 7 moFDA
12,168,036May 10, 2039in 13 yrFDA
11,103,552May 15, 2039in 13 yrFDA
10,973,879May 17, 2039in 13 yrFDA
12,280,093May 17, 2039in 13 yrFDA
D1,035,436Jul 16, 2039in 13 yr 2 moFDA
D1,042,107Sep 17, 2039in 13 yr 4 moFDA
11,850,407Sep 18, 2039in 13 yr 4 moFDA
D1,047,700Oct 22, 2039in 13 yr 5 moFDA
10,961,500Jan 27, 2040in 13 yr 9 moFDA
11,286,460Jan 27, 2040in 13 yr 9 moFDA
11,555,176Jan 27, 2040in 13 yr 9 moFDA
11,821,001Jan 27, 2040in 13 yr 9 moFDA
11,439,758Jun 04, 2040in 14 yr 1 moFDA
11,478,588Jul 25, 2040in 14 yr 3 moFDA
11,160,918Jul 29, 2040in 14 yr 3 moFDA
11,793,926Jul 29, 2040in 14 yr 3 moFDA
11,053,280Aug 18, 2040in 14 yr 4 moFDA
11,104,715Aug 18, 2040in 14 yr 4 moFDA
11,174,283Aug 18, 2040in 14 yr 4 moFDA
11,186,625Aug 18, 2040in 14 yr 4 moFDA
11,299,532Aug 18, 2040in 14 yr 4 moFDA
11,306,135Aug 18, 2040in 14 yr 4 moFDA
11,459,373Aug 18, 2040in 14 yr 4 moFDA
11,459,374Aug 18, 2040in 14 yr 4 moFDA
11,472,861Aug 18, 2040in 14 yr 4 moFDA
11,485,770Aug 18, 2040in 14 yr 4 moFDA
11,505,593Aug 18, 2040in 14 yr 4 moFDA
11,535,663Aug 18, 2040in 14 yr 4 moFDA
11,542,317Aug 18, 2040in 14 yr 4 moFDA
11,548,932Aug 18, 2040in 14 yr 4 moFDA
11,649,273Aug 18, 2040in 14 yr 4 moFDA
11,732,025Aug 18, 2040in 14 yr 4 moFDA
11,753,459Aug 18, 2040in 14 yr 4 moFDA
12,054,533Aug 18, 2040in 14 yr 4 moFDA
12,077,570Aug 18, 2040in 14 yr 4 moFDA
12,202,883Aug 18, 2040in 14 yr 4 moFDA
11,525,833Nov 29, 2040in 14 yr 7 moFDA
12,282,004Dec 09, 2041in 15 yr 7 moFDA
12,163,122May 10, 2042in 16 yr 1 moFDA

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

When do Eylea's patents expire?

The FDA Purple Book lists 88 published patents for Eylea, with the last listed patent expiring May 10, 2042. Every patent below links to its FDA source record so you can verify the expiration date.

Does Eylea have approved biosimilars?

Yes. 6 approved follow-on biologics reference Eylea in the Purple Book: Yesafili, Opuviz, Ahzantive, Enzeevu, Pavblu, and Eydenzelt.

When does Eylea lose reference-product exclusivity?

Eylea's 12-year reference-product exclusivity under the BPCIA is listed in the Purple Book as ending May 18, 2024.

What is Eylea's BLA number?

Eylea is licensed under BLA 125387, held by Regeneron Pharmaceuticals, Inc..

When was Eylea approved by the FDA?

Eylea was first licensed by the FDA on Nov 18, 2011.

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