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Drybench Patent.

ROFLUMILAST, NDA 217242

The patents and exclusivities FDA's Orange Book lists for NDA 217242 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.

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Listed protection

Listed dates run from 15 Dec 2026 to 19 Aug 2042, each by its own rule; no one date stands for this product.

Earliest listed date
15 Dec 2026NP exclusivityRule R3 · Product 001
Source lines

exclusivity.txt line 1,863

Latest listed date
19 Aug 2042US 12,453,721, product patentRule R1 · Product 001
Source lines

patent.txt line 19,833

Latest substance patent
None listed
Latest listed patent
19 Aug 2042US 12,453,721, product patentRule R1 · Product 001
Source lines

patent.txt line 19,833

Latest exclusivity
22 May 2028I-969 exclusivityRule R3 · Product 001
Source lines

exclusivity.txt line 1,862

Listed dates of other NDAs in the same years:20262028203720412042

14 use-code patents, blocking the coded use only

Products

Each product number FDA lists under NDA 217242, as listed. The sections below name products by these numbers.

  • Product 001 · ZORYVE

    Dosage form; route
    FOAM;TOPICAL
    Strength
    0.3%
    Approval date as listed
    15 Dec 2023
    Type as listed
    RX
    Applicant as listed
    ARCUTIS BIOTHERAPEUTICS INC

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.

27 entries from 27 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 10,940,142, product patent

    patent.txt line 19,811
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 11,793,796, product patent

    patent.txt line 19,815
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 11,819,496, use patent

    patent.txt line 19,816
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 11,819,496, use patent

    patent.txt line 19,817
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-4203
    Product numbers
    001
  • US 11,992,480, use patent

    patent.txt line 19,818
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 11,992,480, use patent

    patent.txt line 19,819
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-4203
    Product numbers
    001
  • US 12,005,051, use patent

    patent.txt line 19,820
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 12,005,051, use patent

    patent.txt line 19,821
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-4203
    Product numbers
    001
  • US 12,005,052, product patent

    patent.txt line 19,822
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,011,437, product patent

    patent.txt line 19,823
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,016,848, product patent

    patent.txt line 19,824
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,042,487, product patent

    patent.txt line 19,825
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,220,409, product patent

    patent.txt line 19,826
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,257,242, product patent

    patent.txt line 19,827
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,310,956, use patent

    patent.txt line 19,828
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 12,310,956, use patent

    patent.txt line 19,829
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-4203
    Product numbers
    001
  • US 12,336,983, product patent

    patent.txt line 19,831
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,390,453, product patent

    patent.txt line 19,832
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 12,697,329, product patent

    patent.txt line 19,834
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 9,884,050, product patent

    patent.txt line 19,835
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    product
    Product numbers
    001
  • US 9,907,788, use patent

    patent.txt line 19,836
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 9,907,788, use patent

    patent.txt line 19,837
    Expiry as listed
    7 Jun 2037
    Rule
    R1
    Flags
    use code U-4203
    Product numbers
    001
  • US 11,129,818, use patent

    patent.txt line 19,812
    Expiry as listed
    25 Aug 2037
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 11,129,818, use patent

    patent.txt line 19,813
    Expiry as listed
    25 Aug 2037
    Rule
    R1
    Flags
    use code U-4203
    Product numbers
    001
  • US 11,707,454, use patent

    patent.txt line 19,814
    Expiry as listed
    3 Dec 2041
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 12,329,751, use patent

    patent.txt line 19,830
    Expiry as listed
    3 Dec 2041
    Rule
    R1
    Flags
    use code U-3773
    Product numbers
    001
  • US 12,453,721, product patent

    patent.txt line 19,833
    Expiry as listed
    19 Aug 2042
    Rule
    R1
    Flags
    product
    Product numbers
    001

Listed exclusivities

Each exclusivity FDA lists for NDA 217242, with its code, FDA's definition of the code where the store's code list gives one, and its date as listed.

  • NP exclusivity

    exclusivity.txt line 1,863
    Date
    15 Dec 2026
    Rule
    R3
    Definition
    New product (to be checked against FDA's list)
    Product numbers
    001
  • I-969 exclusivity

    exclusivity.txt line 1,862
    Date
    22 May 2028
    Rule
    R3
    Definition
    New indication (to be checked against FDA's list)
    Product numbers
    001

Paragraph IV list rows giving NDA 217242

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 217242, 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 217242 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