Assyro AI

Orange Book product · Brand (NDA)

YUVIWEL

NAVEPEGRITIDE

Brand (NDA)NDA 219164RX ASCENDIS

At a glance

Feb 27, 2026

Approved

Brand (NDA)

Application

Not listed

TE code

12

Listed patents

Key dates

  1. Approval

    FDA approval date of this drug product.

    Feb 27, 2026

    4 mo ago

  2. Today

  3. Exclusivity ends · NCE

    New chemical entity exclusivity (5 years)

    Feb 27, 2031

    in 4 yr 9 mo

  4. Patent 8906847 expires

    Listed drug substance patent expiration.

    Apr 30, 2031

    in 4 yr 11 mo

  5. Exclusivity ends · ODE-516

    Orphan-drug exclusivity (7 years)

    Feb 27, 2033

    in 6 yr 10 mo

  6. Patent 10835578 expires

    Listed drug substance patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  7. Patent 11154593 expires

    Listed drug substance patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  8. Patent 11224661 expires

    Listed drug substance patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  9. Patent 11311604 expires

    Listed drug substance patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  10. Patent 11389510 expires

    Listed drug substance patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  11. Patent 11389511 expires

    Listed drug product patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  12. Patent 11413351 expires

    Listed drug substance patent expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  13. Patent 12083182 expires

    Listed method-of-use patent (U-4425) expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  14. Patent 12156917 expires

    Listed method-of-use patent (U-4425) expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  15. Patent 12239689 expires

    Listed method-of-use patent (U-4425) expiration.

    Jan 05, 2037

    in 10 yr 8 mo

  16. Patent 12377133 expires

    Listed drug product patent expiration.

    Nov 12, 2042

    in 16 yr 8 mo

Pharmaceutical detail

Active ingredient

NAVEPEGRITIDE

Strength

2.8MG/VIAL

Dosage form

POWDER

Route

SUBCUTANEOUS

TE code

Not listed

Application

NDA 219164

Product number

002

Marketing status

RX

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

Active-ingredient family

View full family

This is a reference-listed drug (RLD) — the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

Marketing exclusivity (2)

  • NCENew chemical entity exclusivity (5 years)

    Feb 27, 2031

    in 4 yr 9 mo

  • ODE-516Orphan-drug exclusivity (7 years)

    Feb 27, 2033

    in 6 yr 10 mo

Listed patents (12)

Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
8906847Apr 30, 2031in 4 yr 11 mo
SubstanceProductU-4425
10835578Jan 05, 2037in 10 yr 8 mo
SubstanceProductU-4425
11154593Jan 05, 2037in 10 yr 8 mo
SubstanceProductU-4425
11224661Jan 05, 2037in 10 yr 8 mo
SubstanceProduct
11311604Jan 05, 2037in 10 yr 8 mo
SubstanceProductU-4425
11389510Jan 05, 2037in 10 yr 8 mo
SubstanceProduct
11389511Jan 05, 2037in 10 yr 8 mo
ProductU-4425
11413351Jan 05, 2037in 10 yr 8 mo
SubstanceProduct
12083182Jan 05, 2037in 10 yr 8 mo
U-4425
12156917Jan 05, 2037in 10 yr 8 mo
U-4425
12239689Jan 05, 2037in 10 yr 8 mo
U-4425
12377133Nov 12, 2042in 16 yr 8 mo
ProductU-4425
Agent CTA Background

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