Zepatier generics — when can they launch?
Zepatier (ELBASVIR) · Merck & Co. · 2 active US patents · 0 expired
Where Zepatier sits in the generic timeline
Imminent generic cliff: earliest active US patent for Zepatier expires in 2029 (~3 years from today). ANDA filers are likely already preparing Paragraph IV certifications. Expect first-filer 180-day exclusivity competition imminently.
Under US Hatch-Waxman, a generic enters via an ANDA (Abbreviated New Drug Application) and may file with one of four Paragraph IV certifications attacking the brand's listed patents. If the brand sues within 45 days, a 30-month FDA approval stay is triggered. First Para IV filer typically gets 180-day market exclusivity.
Patent estate by type — active patents
Method-of-use patents only carve out specific indications; generics can launch with a "skinny label" omitting those uses. Composition-of-matter patents block the molecule itself.
- Method of Use — 2 patents
FDA U-codes carved out by Zepatier patents
Method-of-use patents are listed against specific FDA Patent Use Codes ("U-codes") representing carved-out indications. Generics can launch with a label that omits these uses.
| U-code | Description |
|---|---|
U-1813 | (no description) |
Sample patent estate
Showing 2 of 2 active US patents. View full estate on the Zepatier drug page →
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This patent protects the use of macrocyclic quinoxaline compounds as inhibitors of the hepatitis C virus (HCV) NS3 protease.USPTO title: Macrocyclic quinoxaline compounds as HCV NS3 protease inhibitors
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This patent protects compounds that inhibit hepatitis C virus replication and are useful for treating or preventing HCV infections.USPTO title: Inhibitors of hepatitis C virus replication
Sources
- FDA Orange Book — patents listed against Zepatier (NDA filed 2016)
- Zepatier drug profile — full patent estate, indications, clinical trials, pricing
- Merck & Co. patent portfolio
- Patent cliff 2029 — every drug losing US exclusivity that year
Patent term extensions (PTR, pediatric exclusivity), Hatch-Waxman 30-month stays, and FDA regulatory exclusivity (NCE/ODE/PED) may shift the effective generic entry date. Not legal advice.
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