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Drybench Patent.

TESTOSTERONE ENANTHATE, NDA 209863

The patents and exclusivities FDA's Orange Book lists for NDA 209863 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 appTESTOSTERONE ENANTHATE in the molecule app

Listed protection

Listed dates run from 24 Jan 2026 to 4 Sep 2036, each by its own rule; no one date stands for this product.

Earliest listed date
24 Jan 2026US 10,478,560, product patentRule R1 · Products 001, 002, 003
Source lines

patent.txt lines 10,919, 10,942, 10,965

Latest listed date
4 Sep 2036US 9,950,125, product and use patentRule R1 · Products 001, 002, 003
Source lines

patent.txt lines 10,938, 10,961, 10,984

Latest substance patent
None listed
Latest listed patent
4 Sep 2036US 9,950,125, product and use patentRule R1 · Products 001, 002, 003
Source lines

patent.txt lines 10,938, 10,961, 10,984

Latest exclusivity
None listed

Listed dates of other NDAs in the same years:2026203020312033203420352036

18 use-code patents, blocking the coded use only

Products

Each product number FDA lists under NDA 209863, as listed. The sections below name products by these numbers.

  • Product 001 · XYOSTED (AUTOINJECTOR)

    Dosage form; route
    SOLUTION;SUBCUTANEOUS
    Strength
    50MG/0.5ML (50MG/0.5ML)
    Approval date as listed
    28 Sep 2018
    Type as listed
    RX
    Applicant as listed
    ANTARES PHARMA INC
  • Product 002 · XYOSTED (AUTOINJECTOR)

    Dosage form; route
    SOLUTION;SUBCUTANEOUS
    Strength
    75MG/0.5ML (75MG/0.5ML)
    Approval date as listed
    28 Sep 2018
    Type as listed
    RX
    Applicant as listed
    ANTARES PHARMA INC
  • Product 003 · XYOSTED (AUTOINJECTOR)

    Dosage form; route
    SOLUTION;SUBCUTANEOUS
    Strength
    100MG/0.5ML (100MG/0.5ML)
    Approval date as listed
    28 Sep 2018
    Type as listed
    RX
    Applicant as listed
    ANTARES PHARMA 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.

23 entries from 69 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 10,478,560, product patent

    patent.txt lines 10,919, 10,942, 10,965
    Expiry as listed
    24 Jan 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 11,446,441, product patent

    patent.txt lines 10,927, 10,950, 10,973
    Expiry as listed
    24 Jan 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 8,562,564, product patent

    patent.txt lines 10,933, 10,956, 10,979
    Expiry as listed
    24 Jan 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 9,180,259, product patent

    patent.txt lines 10,934, 10,957, 10,980
    Expiry as listed
    24 Jan 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 9,533,102, product patent

    patent.txt lines 10,935, 10,958, 10,981
    Expiry as listed
    24 Jan 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 9,629,959, product patent

    patent.txt lines 10,936, 10,959, 10,982
    Expiry as listed
    24 Jan 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 8,021,335, product patent

    patent.txt lines 10,932, 10,955, 10,978
    Expiry as listed
    4 Oct 2026
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 11,497,753, product patent

    patent.txt lines 10,928, 10,951, 10,974
    Expiry as listed
    19 Mar 2030
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 10,279,131, product patent

    patent.txt lines 10,917, 10,940, 10,963
    Expiry as listed
    31 Jul 2031
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 10,357,609, product patent

    patent.txt lines 10,918, 10,941, 10,964
    Expiry as listed
    21 Aug 2031
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 10,905,827, product patent

    patent.txt lines 10,922, 10,945, 10,968
    Expiry as listed
    21 Aug 2031
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 11,446,440, product patent

    patent.txt lines 10,926, 10,949, 10,972
    Expiry as listed
    21 Aug 2031
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 10,821,072, product and use patent

    patent.txt lines 10,920, 10,943, 10,966
    Expiry as listed
    4 Jun 2033
    Rule
    R1
    Flags
    product · use code U-2418
    Product numbers
    001, 002, 003
  • US 11,844,804, use patent

    patent.txt lines 10,930, 10,953, 10,976
    Expiry as listed
    4 Jun 2033
    Rule
    R1
    Flags
    use code U-2418
    Product numbers
    001, 002, 003
  • US 10,881,798, product patent

    patent.txt lines 10,921, 10,944, 10,967
    Expiry as listed
    11 Feb 2034
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 11,160,751, product and use patent

    patent.txt lines 10,924, 10,947, 10,970
    Expiry as listed
    7 Oct 2034
    Rule
    R1
    Flags
    product · use code U-2418
    Product numbers
    001, 002, 003
  • US 10,238,662, product and use patent

    patent.txt lines 10,916, 10,939, 10,962
    Expiry as listed
    19 Feb 2035
    Rule
    R1
    Flags
    product · use code U-2418
    Product numbers
    001, 002, 003
  • US 10,912,782, product and use patent

    patent.txt lines 10,923, 10,946, 10,969
    Expiry as listed
    19 Feb 2035
    Rule
    R1
    Flags
    product · use code U-2418
    Product numbers
    001, 002, 003
  • US 11,813,435, product patent

    patent.txt lines 10,929, 10,952, 10,975
    Expiry as listed
    25 Feb 2035
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 12,629,483, product patent

    patent.txt lines 10,931, 10,954, 10,977
    Expiry as listed
    7 Aug 2035
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 11,191,908, product patent

    patent.txt lines 10,925, 10,948, 10,971
    Expiry as listed
    18 Oct 2035
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 9,744,302, product patent

    patent.txt lines 10,937, 10,960, 10,983
    Expiry as listed
    19 Nov 2035
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002, 003
  • US 9,950,125, product and use patent

    patent.txt lines 10,938, 10,961, 10,984
    Expiry as listed
    4 Sep 2036
    Rule
    R1
    Flags
    product · use code U-2418
    Product numbers
    001, 002, 003

Listed exclusivities

Each exclusivity FDA lists for NDA 209863, 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 209863.

Paragraph IV list rows giving NDA 209863

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 209863, 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 209863 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