Drybench Patent.
LOMITAPIDE MESYLATE, NDA 203858
The patents and exclusivities FDA's Orange Book lists for NDA 203858 as captured on 14 October 2026, each date named by its rule and its rows, and any rows of FDA's Paragraph IV list captured on 17 October 2026 that give this NDA's number. Listed protection is a range of dates, never one date.
FDA capture · review pending. Each row is shown as captured from FDA's Orange Book files and Paragraph IV list. Dates are FDA's own; spreadsheet day numbers are shown as dates, and a cell that cannot be read as one date is shown as written and left out of the range. Where FDA lists a *PED row without flags, its flags are read from the base row and marked so. A Paragraph IV row is placed here only by the number in its RLD/NDA cell; nothing is joined by name. How this page reads FDA's files has not been independently reviewed by a regulatory-affairs reviewer.
- Orange Book captured
- 14 October 2026
- Paragraph IV list captured
- 17 October 2026
- Last checked
- 30 October 2026
- Data-branch commit
- dadcab56563716abea6c5e31a5e1970080c778ef
Listed protection is a range of the dates FDA lists, not a forecast of market entry, and not legal, regulatory or investment advice.
Dates as listed in FDA's Orange Book capture of 14 October 2026. This page does not say whether a date has passed; compare it with today's date and FDA's current Orange Book. This page shows only what the capture of 14 October 2026 lists. It does not show patents or exclusivities listed before and since removed.
Listed protection
Listed dates run from 19 Aug 2027 to 29 Jul 2041, each by its own rule; no one date stands for this product.
- Earliest listed date
- 19 Aug 2027US 7,932,268, use patentRule R1 · Products 001, 002, 003, 004, 005, 006, 007
Source lines
patent.txt lines 4,167, 4,169, 4,171, 4,173–4,175, 4,177
- Latest listed date
- 29 Jul 2041US 12,472,172, use patentRule R1 · Products 001, 002, 003, 004, 007
Source lines
patent.txt lines 4,166, 4,168, 4,170, 4,172, 4,176
- Latest substance patent
- None listed
- Latest listed patent
- 29 Jul 2041US 12,472,172, use patentRule R1 · Products 001, 002, 003, 004, 007
Source lines
patent.txt lines 4,166, 4,168, 4,170, 4,172, 4,176
- Latest exclusivity
- 25 Feb 2029NS exclusivityRule R3 · Product 007
Source lines
exclusivity.txt line 347
Listed dates of other NDAs in the same years:202720292041
12 use-code patents, blocking the coded use only
Products
Each product number FDA lists under NDA 203858, as listed. The sections below name products by these numbers.
Product 001 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 5MG BASE
- Approval date as listed
- 21 Dec 2012
- Type as listed
- RX
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Product 002 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 10MG BASE
- Approval date as listed
- 21 Dec 2012
- Type as listed
- RX
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Product 003 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 20MG BASE
- Approval date as listed
- 21 Dec 2012
- Type as listed
- RX
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Product 004 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 30MG BASE
- Approval date as listed
- 23 Apr 2015
- Type as listed
- RX
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Product 005 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 40MG BASE
- Approval date as listed
- 23 Apr 2015
- Type as listed
- DISCN
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Product 006 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 60MG BASE
- Approval date as listed
- 23 Apr 2015
- Type as listed
- DISCN
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Product 007 · JUXTAPID
- Dosage form; route
- CAPSULE;
ORAL - Strength
- EQ 2MG BASE
- Approval date as listed
- 25 Feb 2026
- Type as listed
- RX
- Applicant as listed
- CHIESI FARMACEUTICI SPA
Listed patents
Every patent the FDA lists for this product, as the application holder submitted it, with its flags. The FDA does not verify listings.
2 entries from 12 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.
US 7,932,268, use patent
patent.txt lines 4,167, 4,169, 4,171, 4,173–4,175, 4,177- Expiry as listed
- 19 Aug 2027
- Rule
- R1
- Flags
- use code U-1316
- Product numbers
- 001, 002, 003, 004, 005, 006, 007
US 12,472,172, use patent
patent.txt lines 4,166, 4,168, 4,170, 4,172, 4,176- Expiry as listed
- 29 Jul 2041
- Rule
- R1
- Flags
- use code U-4438
- Product numbers
- 001, 002, 003, 004, 007
Listed exclusivities
Each exclusivity FDA lists for NDA 203858, with its code, FDA's definition of the code where the store's code list gives one, and its date as listed.
NPP exclusivity
exclusivity.txt lines 342–346- Date
- 25 Feb 2029
- Rule
- R3
- Definition
- New patient population (to be checked against FDA's list)
- Product numbers
- 001, 002, 003, 004, 005
NS exclusivity
exclusivity.txt line 347- Date
- 25 Feb 2029
- Rule
- R3
- Definition
- New strength (to be checked against FDA's list)
- Product numbers
- 007
Paragraph IV list rows giving NDA 203858
The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 203858, each cell as listed.
Rows with no NDA number this page can match are kept apart on the list page; some may concern this product.
No row of the Paragraph IV list captured on 17 October 2026 gives NDA 203858 in its RLD/NDA cell. This does not mean no certification was submitted or that no application challenges a patent listed here.
Notes from the trace
- R6 tentative approvals: not in the Orange Book data files as captured; the Drugs@FDA join is a later ruling.
Patents vs FDA exclusivityHow to read the Orange Book data filesParagraph IV certificationWhat changed, by week