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Drybench Patent.

METHYLPHENIDATE HYDROCHLORIDE, NDA 209311

The patents and exclusivities FDA's Orange Book lists for NDA 209311 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.

Open in the appMETHYLPHENIDATE HYDROCHLORIDE in the molecule app

Listed protection

Listed dates run from 23 Mar 2032 to 23 Mar 2032, each by its own rule; no one date stands for this product.

Earliest listed date
23 Mar 2032US 10,182,995, product patentRule R1 · Products 001, 002, 003, 004, 005
Source lines

patent.txt lines 10,078, 10,094, 10,110, 10,126, 10,142

Latest listed date
23 Mar 2032US 9,603,809, use patentRule R1 · Products 001, 002, 003, 004, 005
Source lines

patent.txt lines 10,093, 10,109, 10,125, 10,141, 10,157

Latest substance patent
None listed
Latest listed patent
23 Mar 2032US 9,603,809, use patentRule R1 · Products 001, 002, 003, 004, 005
Source lines

patent.txt lines 10,093, 10,109, 10,125, 10,141, 10,157

Latest exclusivity
None listed

Listed dates of other NDAs in the same years:2032

45 use-code patents, blocking the coded use only

Products

Each product number FDA lists under NDA 209311, as listed. The sections below name products by these numbers.

  • Product 001 · JORNAY PM

    Dosage form; route
    CAPSULE, EXTENDED RELEASE;ORAL
    Strength
    20MG
    Approval date as listed
    8 Aug 2018
    Type as listed
    RX
    Applicant as listed
    IRONSHORE PHARMACEUTICALS INC A WHOLLY OWNED SUB OF COLLEGIUM PHARMACEUTICAL INC
  • Product 002 · JORNAY PM

    Dosage form; route
    CAPSULE, EXTENDED RELEASE;ORAL
    Strength
    40MG
    Approval date as listed
    8 Aug 2018
    Type as listed
    RX
    Applicant as listed
    IRONSHORE PHARMACEUTICALS INC A WHOLLY OWNED SUB OF COLLEGIUM PHARMACEUTICAL INC
  • Product 003 · JORNAY PM

    Dosage form; route
    CAPSULE, EXTENDED RELEASE;ORAL
    Strength
    60MG
    Approval date as listed
    8 Aug 2018
    Type as listed
    RX
    Applicant as listed
    IRONSHORE PHARMACEUTICALS INC A WHOLLY OWNED SUB OF COLLEGIUM PHARMACEUTICAL INC
  • Product 004 · JORNAY PM

    Dosage form; route
    CAPSULE, EXTENDED RELEASE;ORAL
    Strength
    80MG
    Approval date as listed
    8 Aug 2018
    Type as listed
    RX
    Applicant as listed
    IRONSHORE PHARMACEUTICALS INC A WHOLLY OWNED SUB OF COLLEGIUM PHARMACEUTICAL INC
  • Product 005 · JORNAY PM

    Dosage form; route
    CAPSULE, EXTENDED RELEASE;ORAL
    Strength
    100MG
    Approval date as listed
    8 Aug 2018
    Type as listed
    RX
    Applicant as listed
    IRONSHORE PHARMACEUTICALS INC A WHOLLY OWNED SUB OF COLLEGIUM PHARMACEUTICAL 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.

16 entries from 80 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 10,182,995, product patent

    patent.txt lines 10,078, 10,094, 10,110, 10,126, 10,142
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 10,292,937, use patent

    patent.txt lines 10,079, 10,095, 10,111, 10,127, 10,143
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 10,617,651, use patent

    patent.txt lines 10,080, 10,096, 10,112, 10,128, 10,144
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 10,881,618, use patent

    patent.txt lines 10,081, 10,097, 10,113, 10,129, 10,145
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 10,905,652, product patent

    patent.txt lines 10,082, 10,098, 10,114, 10,130, 10,146
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 11,241,391, use patent

    patent.txt lines 10,083, 10,099, 10,115, 10,131, 10,147
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 11,241,392, product patent

    patent.txt lines 10,084, 10,100, 10,116, 10,132, 10,148
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 11,911,518, use patent

    patent.txt lines 10,085, 10,101, 10,117, 10,133, 10,149
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 8,916,588, use patent

    patent.txt lines 10,086, 10,102, 10,118, 10,134, 10,150
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 8,927,010, product patent

    patent.txt lines 10,087, 10,103, 10,119, 10,135, 10,151
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 9,023,389, product patent

    patent.txt lines 10,088, 10,104, 10,120, 10,136, 10,152
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 9,028,868, use patent

    patent.txt lines 10,089, 10,105, 10,121, 10,137, 10,153
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 9,034,902, use patent

    patent.txt lines 10,090, 10,106, 10,122, 10,138, 10,154
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005
  • US 9,283,214, product patent

    patent.txt lines 10,091, 10,107, 10,123, 10,139, 10,155
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 9,498,447, product patent

    patent.txt lines 10,092, 10,108, 10,124, 10,140, 10,156
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003, 004, 005
  • US 9,603,809, use patent

    patent.txt lines 10,093, 10,109, 10,125, 10,141, 10,157
    Expiry as listed
    23 Mar 2032
    Rule
    R1
    Flags
    use code U-2357
    Product numbers
    001, 002, 003, 004, 005

Listed exclusivities

Each exclusivity FDA lists for NDA 209311, with its code, FDA's definition of the code where the store's code list gives one, and its date as listed.

The Orange Book capture of 14 October 2026 lists no exclusivity for NDA 209311.

Paragraph IV list rows giving NDA 209311

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 209311, 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 209311 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