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Drybench Patent.

IVOSIDENIB, NDA 211192

The patents and exclusivities FDA's Orange Book lists for NDA 211192 as captured on 14 October 2026, each date named by its rule and its rows, and the rows of FDA's Paragraph IV list that give this NDA's number, as captured on 17 October 2026. 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.

Open in the appIVOSIDENIB in the molecule app

Listed protection

Listed dates run from 2 May 2026 to 7 Jun 2039, each by its own rule; no one date stands for this product.

Earliest listed date
2 May 2026ODE-242 exclusivityRule R3 · Product 001 · exclusivity.txt line 943
Latest listed date
7 Jun 2039US 10,980,788, use patentRule R1 · Product 001 · patent.txt line 12,523
Latest substance patent
19 Aug 2033US 9,474,779, substance and product and use patentRule R1 · Product 001 · patent.txt line 12,530
Latest listed patent
7 Jun 2039US 10,980,788, use patentRule R1 · Product 001 · patent.txt line 12,523
Latest exclusivity
24 Oct 2030ODE-447 exclusivityRule R3 · Product 001 · exclusivity.txt line 945

30 use-code patents, blocking the coded use only

Products

Each product number FDA lists under NDA 211192, as listed. The sections below name products by these numbers.

  • Product 001 · TIBSOVO

    Dosage form; route
    TABLET;ORAL
    Strength
    250MG
    Approval date as listed
    20 Jul 2018
    Type as listed
    RX
    Applicant as listed
    SERVIER PHARMACEUTICALS LLC

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.

31 entries from 31 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 10,610,125, use patent

    patent.txt line 12,511
    Expiry as listed
    21 Jun 2030
    Rule
    R1
    Flags
    use code U-2784
    Product numbers
    001
  • US 10,610,125, use patent

    patent.txt line 12,512
    Expiry as listed
    21 Jun 2030
    Rule
    R1
    Flags
    use code U-2785
    Product numbers
    001
  • US 10,610,125, use patent

    patent.txt line 12,513
    Expiry as listed
    21 Jun 2030
    Rule
    R1
    Flags
    use code U-3385
    Product numbers
    001
  • US 10,717,764, use patent

    patent.txt line 12,515
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    use code U-3215
    Product numbers
    001
  • US 11,667,673, use patent

    patent.txt line 12,524
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    use code U-3742
    Product numbers
    001
  • US 9,850,277, substance and product and use patent

    patent.txt line 12,531
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    substance · product · use code U-2350
    Product numbers
    001
  • US 9,850,277, substance and product and use patent

    patent.txt line 12,532
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    substance · product · use code U-2533
    Product numbers
    001
  • US 9,850,277, substance and product and use patent

    patent.txt line 12,533
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    substance · product · use code U-2534
    Product numbers
    001
  • US 9,850,277, substance and product and use patent

    patent.txt line 12,534
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    substance · product · use code U-3213
    Product numbers
    001
  • US 9,850,277, substance and product and use patent

    patent.txt line 12,535
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    substance · product · use code U-3386
    Product numbers
    001
  • US 9,850,277, substance and product and use patent

    patent.txt line 12,536
    Expiry as listed
    18 Jan 2033
    Rule
    R1
    Flags
    substance · product · use code U-3742
    Product numbers
    001
  • US 9,474,779, substance and product and use patent

    patent.txt line 12,525
    Expiry as listed
    19 Aug 2033
    Rule
    R1
    Flags
    substance · product · use code U-2350
    Product numbers
    001
  • US 9,474,779, substance and product and use patent

    patent.txt line 12,526
    Expiry as listed
    19 Aug 2033
    Rule
    R1
    Flags
    substance · product · use code U-2533
    Product numbers
    001
  • US 9,474,779, substance and product and use patent

    patent.txt line 12,527
    Expiry as listed
    19 Aug 2033
    Rule
    R1
    Flags
    substance · product · use code U-2534
    Product numbers
    001
  • US 9,474,779, substance and product and use patent

    patent.txt line 12,528
    Expiry as listed
    19 Aug 2033
    Rule
    R1
    Flags
    substance · product · use code U-3213
    Product numbers
    001
  • US 9,474,779, substance and product and use patent

    patent.txt line 12,529
    Expiry as listed
    19 Aug 2033
    Rule
    R1
    Flags
    substance · product · use code U-3386
    Product numbers
    001
  • US 9,474,779, substance and product and use patent

    patent.txt line 12,530
    Expiry as listed
    19 Aug 2033
    Rule
    R1
    Flags
    substance · product · use code U-3742
    Product numbers
    001
  • US 10,449,184, product patent

    patent.txt line 12,510
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 10,799,490, product and use patent

    patent.txt line 12,516
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-2981
    Product numbers
    001
  • US 10,799,490, product and use patent

    patent.txt line 12,517
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-2982
    Product numbers
    001
  • US 10,799,490, product and use patent

    patent.txt line 12,518
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-3384
    Product numbers
    001
  • US 9,968,595, product and use patent

    patent.txt line 12,537
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-2351
    Product numbers
    001
  • US 9,968,595, product and use patent

    patent.txt line 12,538
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-2533
    Product numbers
    001
  • US 9,968,595, product and use patent

    patent.txt line 12,539
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-2534
    Product numbers
    001
  • US 9,968,595, product and use patent

    patent.txt line 12,540
    Expiry as listed
    13 Mar 2035
    Rule
    R1
    Flags
    product · use code U-3384
    Product numbers
    001
  • US 10,653,710, use patent

    patent.txt line 12,514
    Expiry as listed
    18 Oct 2036
    Rule
    R1
    Flags
    use code U-3387
    Product numbers
    001
  • US 10,980,788, use patent

    patent.txt line 12,519
    Expiry as listed
    7 Jun 2039
    Rule
    R1
    Flags
    use code U-3112
    Product numbers
    001
  • US 10,980,788, use patent

    patent.txt line 12,520
    Expiry as listed
    7 Jun 2039
    Rule
    R1
    Flags
    use code U-3113
    Product numbers
    001
  • US 10,980,788, use patent

    patent.txt line 12,521
    Expiry as listed
    7 Jun 2039
    Rule
    R1
    Flags
    use code U-3214
    Product numbers
    001
  • US 10,980,788, use patent

    patent.txt line 12,522
    Expiry as listed
    7 Jun 2039
    Rule
    R1
    Flags
    use code U-3383
    Product numbers
    001
  • US 10,980,788, use patent

    patent.txt line 12,523
    Expiry as listed
    7 Jun 2039
    Rule
    R1
    Flags
    use code U-3743
    Product numbers
    001

Listed exclusivities

Each exclusivity FDA lists for NDA 211192, with its code, FDA's definition of the code where the store's code list gives one, and its date as listed.

  • ODE-242 exclusivity

    exclusivity.txt line 943
    Date
    2 May 2026
    Rule
    R3
    Definition
    Orphan drug exclusivity (to be checked against FDA's list)
    Product numbers
    001
  • I-924 exclusivity

    exclusivity.txt line 942
    Date
    24 Oct 2026
    Rule
    R3
    Definition
    New indication (to be checked against FDA's list)
    Product numbers
    001
  • ODE-368 exclusivity

    exclusivity.txt line 944
    Date
    25 Aug 2028
    Rule
    R3
    Definition
    Orphan drug exclusivity (to be checked against FDA's list)
    Product numbers
    001
  • ODE-447 exclusivity

    exclusivity.txt line 945
    Date
    24 Oct 2030
    Rule
    R3
    Definition
    Orphan drug exclusivity (to be checked against FDA's list)
    Product numbers
    001

Paragraph IV list rows giving NDA 211192

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 211192, each cell as listed.

FDA's Paragraph IV list names no patent number, so it does not say which of the patents on this page an applicant certified against.

The list gives the last qualifying patent's expiry without pediatric exclusivity; in the app's Patents view, the Orange Book lists any *PED period as a separate row with its own date. The two dates describe different things. A blank cell is one FDA left blank in its list. Dates are FDA's own; the last qualifying patent expiry is not recomputed from the Orange Book.

Rows whose RLD/NDA cell we could not read as exactly one NDA number are kept apart on the list page; some may concern this product.

Rows on FDA's Paragraph IV list whose RLD/NDA cell gives NDA 211192

  • Ivosidenib · Tablets · 250 mg

    RLD/NDA as listed: Tibsovo 211192
    First PIV submission
    20 Jul 2022
    ANDAs
    1
    180-day status
    blank
    Decision posted
    blank
    First applicant approval
    blank
    First marketing
    blank
    Last qualifying patent expiry (as listed by FDA)
    7 Jun 2039

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