tirzepatide · Eli Lilly And Co · NDA 217806

Zepbound Kwikpen

Earliest generic entry, as listed · earliest of 6 marketed strengths
22 Jul 2039

Blocked by patent: US 12343382, US 12453758, US 12616740. Only method-of-use patents remain, so a generic may carve out the protected indication and enter earlier.

Listed patents · 4 unexpired

12 Orange Book listing rows for 4 patents. FDA lists a patent once for each use code, and lists its pediatric extension as a separate row.

PatentClaimsExpires
US 12343382use U-4227, U-4228, U-4409, U-441022 Jul 2039
US 12343382 listing rowuse U-4227 · sets the listed date22 Jul 2039
US 12343382 listing rowuse U-4228 · sets the listed date22 Jul 2039
US 12343382 listing rowuse U-4409 · sets the listed date22 Jul 2039
US 12343382 listing rowuse U-4410 · sets the listed date22 Jul 2039
US 12453758use U-4308, U-4309, U-4310, U-431122 Jul 2039
US 12453758 listing rowuse U-4308 · sets the listed date22 Jul 2039
US 12453758 listing rowuse U-4309 · sets the listed date22 Jul 2039
US 12453758 listing rowuse U-4310 · sets the listed date22 Jul 2039
US 12453758 listing rowuse U-4311 · sets the listed date22 Jul 2039
US 12616740use U-4497, U-4498, U-449922 Jul 2039
US 12616740 listing rowuse U-4497 · sets the listed date22 Jul 2039
US 12616740 listing rowuse U-4498 · sets the listed date22 Jul 2039
US 12616740 listing rowuse U-4499 · sets the listed date22 Jul 2039
US 9474780drug substance, drug product13 May 2036

Exclusivities · 3 unexpired

I-958new indication (3 years)20 Dec 2027
M-82miscellaneous (3 years)18 Oct 2027
NCEnew chemical entity (5 years)13 May 2027

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 · 6

NDA · productFormStrengthListed expiry
217806 · 019 · RLDsolution, subcutaneous10MG/2.4ML (4.17MG/ML)22 Jul 2039
217806 · 020 · RLDsolution, subcutaneous20MG/2.4ML (8.33MG/ML)22 Jul 2039
217806 · 021 · RLDsolution, subcutaneous30MG/2.4ML (12.5MG/ML)22 Jul 2039
217806 · 022 · RLDsolution, subcutaneous40MG/2.4ML (16.7MG/ML)22 Jul 2039
217806 · 023 · RLDsolution, subcutaneous50MG/2.4ML (20.8MG/ML)22 Jul 2039
217806 · 024 · RLDsolution, subcutaneous60MG/2.4ML (25MG/ML)22 Jul 2039