ruxolitinib phosphate · Incyte Corp · NDA 217180

Jakafi Xr

Earliest generic entry, as listed · earliest of 5 marketed strengths
17 Jul 2034

Blocked by patent: US 11337927.

Listed patents · 53 unexpired

PatentClaimsExpires
US 11337927—17 Jul 2034
US 10874616—14 May 2034
US 11576864—14 May 2034
US 11576865—14 May 2034
US 11896717—14 May 2034
US 11337927use U-323017 Jan 2034
US 11337927use U-322617 Jan 2034
US 11337927use U-322817 Jan 2034
US 11337927use U-322717 Jan 2034
US 10874616product14 Nov 2033
US 11576864use U-323014 Nov 2033
US 11576864use U-322714 Nov 2033
US 11576864use U-322814 Nov 2033
US 11576864use U-322614 Nov 2033
US 11576865product, use U-322714 Nov 2033
US 11576865product, use U-322814 Nov 2033
US 11576865product, use U-323014 Nov 2033
US 11576865product, use U-322614 Nov 2033
US 11896717product, use U-322814 Nov 2033
US 11896717product, use U-322614 Nov 2033
US 11896717product, use U-323014 Nov 2033
US 11896717product, use U-322714 Nov 2033
US 10016429—12 Dec 2028
US 11213528—12 Dec 2028
US 8722693—12 Dec 2028
US 8822481—12 Dec 2028
US 8829013—12 Dec 2028
US 7598257—24 Jun 2028
US 8415362—24 Jun 2028
US 10016429use U-322612 Jun 2028
US 10016429use U-323012 Jun 2028
US 11213528product12 Jun 2028
US 8722693substance, product12 Jun 2028
US 8822481use U-322712 Jun 2028
US 8822481use U-322812 Jun 2028
US 8822481use U-323012 Jun 2028
US 8822481use U-322612 Jun 2028
US 8829013use U-322712 Jun 2028
US 8829013use U-322812 Jun 2028
US 7598257substance, product, use U-322824 Dec 2027
US 7598257substance, product, use U-322724 Dec 2027
US 8415362substance, product24 Dec 2027
US 11744832use U-323012 Dec 2026
US 11744832use U-322612 Dec 2026
US 8530485product12 Dec 2026
US 9079912use U-322612 Dec 2026
US 9079912use U-322812 Dec 2026
US 9079912use U-322712 Dec 2026
US 9079912use U-323012 Dec 2026
US 9206187use U-322712 Dec 2026
US 9206187use U-322812 Dec 2026
US 9814722use U-323012 Dec 2026
US 9814722use U-322612 Dec 2026

Exclusivities · 2 unexpired

PEDpediatric (6 months added)22 Mar 2029
ODE*22 Sep 2028

Paragraph IV certifications · 0

No Paragraph IV certification listed by FDA for this drug.

The list shows that a generic applicant certified to FDA that a listed patent is invalid or not infringed. It does not show litigation, settlements or launch timing.

Event history

No events yet. The first ingestion only records products entering their 12-month window; changes appear from the next Orange Book update.

Products covered · 5

NDA · productFormStrengthListed expiry
217180 · 001 · RLDtablet, extended release, oralEQ 11MG BASE17 Jul 2034
217180 · 002 · RLDtablet, extended release, oralEQ 22MG BASE17 Jul 2034
217180 · 003 · RLDtablet, extended release, oralEQ 33MG BASE17 Jul 2034
217180 · 004 · RLDtablet, extended release, oralEQ 44MG BASE17 Jul 2034
217180 · 005 · RLDtablet, extended release, oralEQ 55MG BASE17 Jul 2034