Assyro AI

FDA Orange Book · active-ingredient family

Ubrogepant

Ubrogepant is approved in 1 FDA application, with therapeutic-equivalence codes, listed patents, and marketing exclusivity from the FDA Orange Book.

Reference-listed drug:UBRELVY · NDA 211765

1

Brand (NDA)

0

Generics (ANDA)

16

Listed patents

0

Exclusivity periods

Brand (NDA) products · tablet

ProductApplicantApplicationTEApproved
UBRELVYRLD×2ABBVIENDA 211765Dec 23, 2019

Listed patents (16)

Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
9499545Nov 10, 2031in 5 yr 6 mo
SubstanceProductU-2718
9833448Nov 10, 2031in 5 yr 6 mo
U-2718
8754096Jul 19, 2032in 6 yr 2 mo
SubstanceProductU-2717
8912210Dec 23, 2033in 7 yr 7 mo
SubstanceProduct
12220408Jan 30, 2035in 8 yr 9 mo
Product
12458632Jan 30, 2035in 8 yr 9 mo
Product
11925709Jan 30, 2035in 8 yr 9 mo
Product
12168004Jan 30, 2035in 8 yr 9 mo
Product
10117836Jan 30, 2035in 8 yr 9 mo
Product
12310953Jan 30, 2035in 8 yr 9 mo
Product
12458633Jan 30, 2035in 8 yr 9 mo
Product
11717515Dec 22, 2041in 15 yr 9 mo
U-3677
12329750Dec 22, 2041in 15 yr 9 mo
U-4213
12194030Dec 22, 2041in 15 yr 9 mo
U-4121
11857542Dec 22, 2041in 15 yr 9 mo
U-3786
12070450Dec 22, 2041in 15 yr 9 mo
U-3992

Ubrogepant — frequently asked questions

Generics, reference-listed drug, patents, and exclusivity for this active ingredient, from the FDA Orange Book.

Agent CTA Background

Your Next Submission Could Take 6+ Fewer Weeks and Cost $250K Less.